Benzopyrazole compounds and analogues thereof

ABSTRACT

Disclosed are compounds of formula I, and pharmaceutically acceptable salts thereof. The compounds are inhibitors of the complement system. Also provided are pharmaceutical compositions comprising a compound of formula I, and methods involving use of the compounds and compositions in the treatment and prevention of diseases and conditions characterized by aberrant complement system activity.

RELATED APPLICATIONS

This application claims the benefit of priority to U.S. Provisionalpatent Application Ser. No. 62/289,653, filed Feb. 1, 2016, the contentsof which are hereby incorporated by reference.

BACKGROUND OF THE INVENTION

The complement system is a branch of an organism's immune system thatenhances the ability of antibodies and phagocytic cells to destroy andremove foreign particles (e.g., pathogens) from the organism. Thecomplement system comprises a set of plasma proteins that act togetherto attack extracellular forms of pathogens and induce a series ofinflammatory responses to help fight infection. Complement activationcan occur through several pathways. For example, complement activationcan occur spontaneously in response to certain pathogens or by antibodybinding to a pathogen. When complement proteins are activated a cascadeis triggered by which one complement protein induces the activation ofthe next protein in the sequence. The activation of a small number ofcomplement proteins at the start of the pathway is hugely amplified byeach successive enzymatic reaction, resulting in the rapid generation ofa disproportionately large complement response. (Marrides, S.Pharmacological Reviews 1998, Vol. 50, pages 59-88). In healthyorganisms there are regulatory mechanisms to prevent uncontrolledcomplement activation.

When activated, complement proteins can bind to a pathogen, opsonizingthem for engulfment by phagocytes bearing receptors for complement.Then, small fragments of some complement proteins act aschemoattractants to recruit more phagocytes to the site of complementactivation, and also to activate these phagocytes. Next, the complementproteins create holes or pores in the invading organisms, leading totheir destruction. While complement plays an important role inprotecting the body from foreign organisms, it can also destroy healthycells and tissue. The inappropriate activation of complement isimplicated in a long list of disease pathologies (Morgan, B. Eur J ClinInvest 1994, Vol. 24, pages 219-228) affecting the immune, renal,cardiovascular, and neurological systems.

SUMMARY OF THE INVENTION

In certain aspects, the invention provides compounds of formula (I), andpharmaceutically acceptable salts thereof:

wherein, independently for each occurrence:

-   -   R¹ represents optionally substituted aryl, heteroaryl,        cycloalkyl, heterocycloalkyl, alkyl, or alkenyl;    -   R² and R³ each independently represent H, F, or optionally        substituted alkyl, alkenyl, alkynyl, alkoxyalkyl, haloalkyl,        hydroxyalkyl, (alkylthio)alkyl, aralkyl, heteroaralkyl,        cycloalkyl, (cycloalkyl)alkyl, heterocycloalkyl, or        (heterocycloalkyl)alkyl;    -   or R² and R³, taken together with the carbon atom to which they        are bonded, form an optionally substituted cycloalkyl or        heterocycloalkyl ring;    -   R⁴ represents H or optionally substituted alkyl, alkenyl,        alkynyl, cycloalkyl, (cycloalkyl)alkyl, heterocycloalkyl,        (heterocycloalkyl)alkyl, aralkyl, heteroaralkyl, hydroxyalkyl,        or haloalkyl;    -   X represents NH, CH₂, CHF, CF₂, CH(C₁-C₆)alkyl, or        C((C₁-C₆)alkyl)₂;    -   Y is absent or represents CH₂, C(O), CR¹⁵R¹⁶, S(O)₂, or        optionally substituted (C₃-C₇)cycloalkylene, arylene, or        heteroarylene;    -   R^(a) represents H or optionally substituted (C₁-C₆)alkyl,        (heterocycloalkyl)alkyl, or (C₃-C₇)cycloalkyl;    -   m is an integer from 1-6;    -   n is 0 or 1;    -   R¹⁵ and R¹⁶ are each independently selected from the group        consisting of H, hydroxy, halogen, —C(O)OR¹⁷, —C(O)NR¹⁷R¹⁸,        —NR¹⁷R¹⁸, alkyl, hydroxyalkyl, haloalkyl, alkoxyalkyl, aryl,        aralkyl, heteroaryl, heteroaralkyl, cycloalkyl,        (cycloalkyl)alkyl, heterocycloalkyl, and        (heterocycloalkyl)alkyl, wherein alkyl, aryl, aralkyl,        heteroaryl, heteroaralkyl, cycloalkyl, (cycloalkyl)alkyl,        heterocycloalkyl, and (heterocycloalkyl)alkyl are optionally        substituted with one or more substituents selected from the        group consisting of —CN, —OR¹⁷, —NR¹⁷R¹⁸, halo, and alkyl;    -   or R¹⁵ and R¹⁶ may be taken together with the intervening atom        to form an optionally substituted carbocyclic or heterocyclic        ring;    -   R¹⁷ and R¹⁸ are each independently selected from the group        consisting of H, alkyl, haloalkyl, hydroxyalkyl, alkoxyalkyl,        aryl, aralkyl, heteroaryl, heteroaralkyl, cycloalkyl,        (cycloalkyl)alkyl, heterocycloalkyl, and        (heterocycloalkyl)alkyl;    -   or R¹⁷ and R¹⁸, when attached to the same atom, may be taken        together with the intervening atom to form an optionally        substituted heterocyclic ring;

represents

-   -   Z¹ and Z³ each independently represent C or N;    -   Z² represents N, CH, or CF;    -   Z⁴ represents N or CR⁸;    -   Z⁵ represents N or CR⁵;    -   Z⁶ represents N or CR⁶;    -   Z⁷ represents N or CR⁹;    -   Z⁸ and Z⁹ each independently represent N or CR¹⁹;    -   R⁵ and R⁶ each independently represent H, halogen, —CN, —NO₂,        —OR¹³, —NR¹³R¹⁴, —C(O)R¹³, —C(O)OR¹³, —C(O)NR¹³R¹⁴, —OC(O)R¹³,        —NR¹³C(O)R¹⁴, —OC(O)NR¹³R¹⁴, —OC(O)OR¹³, —NR¹³C(O)OR¹⁴,        —NR¹³C(O)NR¹³R¹⁴, —OS(O)_(p)(R¹³), —NR¹³S(O)_(p)(R¹⁴), or        optionally substituted alkyl, alkenyl, alkynyl, haloalkyl,        aralkyl, heteroaralkyl, heteroaryl, aryl, cycloalkyl,        (cycloalkyl)alkyl, heterocycloalkyl, or (heterocycloalkyl)alkyl;    -   L represents —H, —CN, —C(O)R⁷, —CH(OH)R⁷, or —S(O)_(p)(alkyl);    -   R⁷, independently for each occurrence, represents H, NH₂, CH₃,        OH, CF₃, CH₂OH, (C₁-C₆)alkyl, hydroxy(C₁-C₆)alkyl,        (C₁-C₆)alkoxy(C₁-C₆)alkyl, halo(C₁-C₆)alkyl, NH(C₁-C₆)alkyl,        N((C₁-C₆)alkyl)₂;    -   R⁸ and R⁹ each independently represent H, halogen, —OR¹³,        —NR¹³R¹⁴, —C(O)R¹³, —C(O)OR¹³, —C(O)NR¹³R¹⁴, —OC(O)R¹³,        —NR¹³C(O)R¹⁴, —OC(O)NR¹³R¹⁴, —OC(O)OR¹³, —NR¹³C(O)OR¹⁴,        —NR¹³C(O)NR¹³R¹⁴, —OS(O)_(p)(R¹³), —NR¹³S(O)_(p)(R¹⁴), or        optionally substituted alkyl, alkenyl, alkynyl, haloalkyl,        aralkyl, heteroaralkyl, heteroaryl, or aryl;    -   or R⁵ and R⁸, or R⁵ and R⁶, or R⁶ and R⁹ may be taken together        with the intervening atoms to form an optionally substituted        heterocyclic or carbocyclic ring;    -   R¹³ and R¹⁴, independently for each occurrence, represent H or        optionally substituted alkyl, alkenyl, alkynyl, aryl, aralkyl,        heteroaryl, heteroaralkyl, cycloalkyl, (cycloalkyl)alkyl,        heterocycloalkyl, or (heterocycloalkyl)alkyl; or, when R¹³ and        RH are attached to the same atom, R¹³ and R¹⁴ taken together        with the atom may form an optionally substituted heterocyclic        ring;    -   R¹⁹, independently for each occurrence, represents H, F, CN,        —C(O)R⁷, —CH(OH)R⁷, or S(O)_(p)(alkyl);    -   J represents H or NH₂; and    -   p is 0, 1, or 2;    -   wherein, if Z¹ is N, or if

represents

then X represents CH₂.

In certain aspects, the invention provides a pharmaceutical composition,comprising a compound of the invention, or a pharmaceutically acceptablesalt thereof; and a pharmaceutically acceptable carrier.

In certain aspects, the invention provides a method of treating orpreventing a disease or condition characterized by aberrant complementsystem activity. The method comprises the step of administering to asubject in need thereof a therapeutically effective amount of a compoundof the invention, or a pharmaceutically acceptable salt thereof, therebytreating or preventing the disease or condition characterized byaberrant complement system activity. In certain embodiments, the diseaseor condition characterized by aberrant complement system activity is animmunological disorder. In certain embodiments, the disease or conditioncharacterized by aberrant complement system activity is a disease of thecentral nervous system. In certain embodiments, the disease or conditioncharacterized by aberrant complement system activity is aneurodegenerative disease or neurological disease. In certainembodiments, the disease or condition characterized by aberrantcomplement system activity is a renal disease. In certain embodiments,the disease or condition characterized by aberrant complement systemactivity is a cardiovascular disease. In certain embodiments, thedisease or condition characterized by aberrant complement systemactivity is selected from the group consisting of paroxysmal nocturnalhemoglobinuria, atypical hemolytic uremic syndrome, organ transplantrejection, myasthenia gravis, neuromyelitis optica,membranoproliferative glomerulonephritis, dense-deposit disease, coldagglutinin disease, and catastrophic antiphospholipid syndrome.

DETAILED DESCRIPTION

Inhibitors of the complement system have been reported and are useful intherapeutic methods and compositions suitable for use in treating orpreventing various immunological disorders, eurodegenerative diseases,and diseases of the central nervous system. Provided herein arecompounds of formula (I) that are useful treating or preventing adisease or condition characterized by aberrant complement systemactivity.

Definitions

The articles “a” and “an” are used herein to refer to one or to morethan one (i.e., to at least one) of the grammatical object of thearticle. By way of example, “an element” means one element or more thanone element.

The term “heteroatom” is art-recognized and refers to an atom of anyelement other than carbon or hydrogen. Illustrative heteroatoms includeboron, nitrogen, oxygen, phosphorus, sulfur and selenium, andalternatively oxygen, nitrogen or sulfur.

The term “alkyl” as used herein is a term of art and refers to saturatedaliphatic groups, including straight-chain alkyl groups, branched-chainalkyl groups, cycloalkyl (alicyclic) groups, alkyl substitutedcycloalkyl groups, and cycloalkyl substituted alkyl groups. In certainembodiments, a straight-chain or branched-chain alkyl has about 30 orfewer carbon atoms in its backbone (e.g., C₁-C₃₀ for straight chain,C₃-C₃₀ for branched chain), and alternatively, about 20 or fewer, or 10or fewer. In certain embodiments, the term “alkyl” refers to a C₁-C₁₀alkyl group. In certain embodiments, the term “alkyl” refers to a C₁-C₆alkyl group, for example a C₁-C₆ straight-chain alkyl group. In certainembodiments, the term “alkyl” refers to a C₃-C₁₂ branched-chain alkylgroup. In certain embodiments, the term “alkyl” refers to a C₃-C₈branched-chain alkyl group. Representative examples of alkyl include,but are not limited to, methyl, ethyl, n-propyl, iso-propyl, n-butyl,sec-butyl, iso-butyl, tert-butyl, n-pentyl, isopentyl, neopentyl, andn-hexyl.

The term “cycloalkyl” means mono- or bicyclic or bridged saturatedcarbocyclic rings, each having from 3 to 12 carbon atoms. Certaincycloalkyls have from 5-12 carbon atoms in their ring structure, and mayhave 6-10 carbons in the ring structure. Preferably, cycloalkyl is(C₃-C₇)cycloalkyl, which represents a monocyclic saturated carbocyclicring, having from 3 to 7 carbon atoms. Examples of monocycliccycloalkyls include cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl,cyclohexyl, cyclohexenyl, cycloheptyl, and cyclooctyl. Bicycliccycloalkyl ring systems include bridged monocyclic rings and fusedbicyclic rings. Bridged monocyclic rings contain a monocyclic cycloalkylring where two non-adjacent carbon atoms of the monocyclic ring arelinked by an alkylene bridge of between one and three additional carbonatoms (i.e., a bridging group of the form —(CH₂)_(w)—, where w is 1, 2,or 3). Representative examples of bicyclic ring systems include, but arenot limited to, bicyclo[3.1.1]heptane, bicyclo[2.2.1]heptane,bicyclo[2.2.2]octane, bicyclo[3.2.2]nonane, bicyclo[3.3.1]nonane, andbicyclo[4.2.1]nonane. Fused bicyclic cycloalkyl ring systems contain amonocyclic cycloalkyl ring fused to either a phenyl, a monocycliccycloalkyl, a monocyclic cycloalkenyl, a monocyclic heterocyclyl, or amonocyclic heteroaryl. The bridged or fused bicyclic cycloalkyl isattached to the parent molecular moiety through any carbon atomcontained within the monocyclic cycloalkyl ring. Cycloalkyl groups areoptionally substituted. In certain embodiments, the fused bicycliccycloalkyl is a 5 or 6 membered monocyclic cycloalkyl ring fused toeither a phenyl ring, a 5 or 6 membered monocyclic cycloalkyl, a 5 or 6membered monocyclic cycloalkenyl, a 5 or 6 membered monocyclicheterocyclyl, or a 5 or 6 membered monocyclic heteroaryl, wherein thefused bicyclic cycloalkyl is optionally substituted.

The term “(cycloalkyl)alkyl” as used herein refers to an alkyl groupsubstituted with one or more cycloalkyl groups. An example ofcycloalkylalkyl is cyclohexylmethyl group.

The term “heterocycloalkyl” as used herein refers to a radical of anon-aromatic ring system, including, but not limited to, monocyclic,bicyclic, and tricyclic rings, which can be completely saturated orwhich can contain one or more units of unsaturation, for the avoidanceof doubt, the degree of unsaturation does not result in an aromatic ringsystem, and having 3 to 12 atoms including at least one heteroatom, suchas nitrogen, oxygen, or sulfur. For purposes of exemplification, whichshould not be construed as limiting the scope of this invention, thefollowing are examples of heterocyclic rings: aziridinyl, azirinyl,oxiranyl, thiiranyl, thiirenyl, dioxiranyl, diazirinyl, diazepanyl,1,3-dioxanyl, 1,3-dioxolanyl, 1,3-dithiolanyl, 1,3-dithianyl,imidazolidinyl, isothiazolinyl, isothiazolidinyl, isoxazolinyl,isoxazolidinyl, azetyl, oxetanyl, oxetyl, thietanyl, thietyl,diazetidinyl, dioxetanyl, dioxetenyl, dithietanyl, dithietyl,dioxalanyl, oxazolyl, thiazolyl, triazinyl, isothiazolyl, isoxazolyl,azepines, azetidinyl, morpholinyl, oxadiazolinyl, oxadiazolidinyl,oxazolinyl, oxazolidinyl, oxopiperidinyl, oxopyrrolidinyl, piperazinyl,piperidinyl, pyranyl, pyrazolinyl, pyrazolidinyl, pyrrolinyl,pyrrolidinyl, quinuclidinyl, thiomorpholinyl, tetrahydropyranyl,tetrahydrofuranyl, tetrahydrothienyl, thiadiazolinyl, thiadiazolidinyl,thiazolinyl, thiazolidinyl, thiomorpholinyl, 1,1-dioxidothiomorpholinyl(thiomorpholine sulfone), thiopyranyl, and trithianyl. Aheterocycloalkyl group is optionally substituted by one or moresubstituents as described below.

The term “(heterocycloalkyl)alkyl” as used herein refers to an alkylgroup substituted with one or more heterocycloalkyl (i.e., heterocyclyl)groups.

The term “alkenyl” as used herein means a straight or branched chainhydrocarbon radical containing from 2 to 10 carbons and containing atleast one carbon-carbon double bond formed by the removal of twohydrogens. Representative examples of alkenyl include, but are notlimited to, ethenyl, 2-propenyl, 2-methyl-2-propenyl, 3-butenyl,4-pentenyl, 5-hexenyl, 2-heptenyl, 2-methyl-1-heptenyl, and 3-decenyl.The unsaturated bond(s) of the alkenyl group can be located anywhere inthe moiety and can have either the (Z) or the (E) configuration aboutthe double bond(s).

The term “alkynyl” as used herein means a straight or branched chainhydrocarbon radical containing from 2 to 10 carbon atoms and containingat least one carbon-carbon triple bond. Representative examples ofalkynyl include, but are not limited, to acetylenyl, 1-propynyl,2-propynyl, 3-butynyl, 2-pentynyl, and 1-butynyl.

The term “alkylene” is art-recognized, and as used herein pertains to adiradical obtained by removing two hydrogen atoms of an alkyl group, asdefined above. In one embodiment an alkylene refers to a disubstitutedalkane, i.e., an alkane substituted at two positions with substituentssuch as halogen, azide, alkyl, aralkyl, alkenyl, alkynyl, cycloalkyl,hydroxyl, alkoxyl, amino, nitro, sulthydryl, imino, amido, phosphonate,phosphinate, carbonyl, carboxyl, silyl, ether, alkylthio, sulfonyl,sulfonamido, ketone, aldehyde, ester, heterocyclyl, aromatic orheteroaromatic moieties, fluoroalkyl (such as trifluromethyl), cyano, orthe like. That is, in one embodiment, a “substituted alkyl” is an“alkylene”.

The term “amino” is a term of art and as used herein refers to bothunsubstituted and substituted amines, e.g., a moiety that may berepresented by the general formulas:

wherein R_(a), R_(b), and R_(c) each independently represent a hydrogen,an alkyl, an alkenyl, —(CH₂)_(x)—R_(d), or R_(a) and R_(b), takentogether with the N atom to which they are attached complete aheterocycle having from 4 to 8 atoms in the ring structure; Rdrepresents an aryl, a cycloalkyl, a cycloalkenyl, a heterocyclyl or apolycyclyl; and x is zero or an integer in the range of 1 to 8. Incertain embodiments, only one of R_(a) or R_(b) may be a carbonyl, e.g.,R_(a), R_(b), and the nitrogen together do not form an imide. In otherembodiments, R_(a) and R_(b) (and optionally R_(c)) each independentlyrepresent a hydrogen, an alkyl, an alkenyl, or —(CH₂)_(x)—R_(d).

In certain embodiments, the term “amino” refers to NH₂.

In certain embodiments, the term “alkylamino” refers to —NH(alkyl).

In certain embodiments, the term “dialkylamino” refers to —N(alkyl)₂.

The term “amido”, as used herein, means —NHC(═O)—, wherein the amidogroup is bound to the parent molecular moiety through the nitrogen.Examples of amido include alkylamido such as CH₃C(═O)N(H)— andCH₃CH₂C(═O)N(H)—.

The term “acyl” is a term of art and as used herein refers to any groupor radical of the form RCO— where R is any organic group, e.g., alkyl,aryl, heteroaryl, aralkyl, and heteroaralkyl. Representative acyl groupsinclude acetyl, benzoyl, and malonyl.

The term “aminoalkyl” as used herein refers to an alkyl groupsubstituted with one or more one amino groups. In one embodiment, theterm “aminoalkyl” refers to an aminomethyl group.

The term “aminoacyl” is a term of art and as used herein refers to anacyl group substituted with one or more amino groups.

The term “aminothionyl” as used herein refers to an analog of anaminoacyl in which the O of RC(O)— has been replaced by sulfur, hence isof the form RC(S)—.

The term “phosphoryl” is a term of art and as used herein may in generalbe represented by the formula:

wherein Q50 represents S or O, and R59 represents hydrogen, a loweralkyl or an aryl; for example, —P(O)(OMe)- or —P(O)(OH)₂. When used tosubstitute, e.g., an alkyl, the phosphoryl group of the phosphorylalkylmay be represented by the general formulas:

wherein Q50 and R59, each independently, are defined above, and Q51represents 0, S or N; for example, —O—P(O)(OH)OMe or —NH—P(O)(OH)₂. WhenQ50 is S, the phosphoryl moiety is a “phosphorothioate.”

The term “aminophosphoryl” as used herein refers to a phosphoryl groupsubstituted with at least one amino group, as defined herein; forexample, —P(O)(OH)NMe₂.

The term “azide” or “azido”, as used herein, means an N3 group.

The term “carbonyl” as used herein refers to —C(═O)—.

The term “thiocarbonyl” as used herein refers to —C(═S)—.

The term “alkylphosphoryl” as used herein refers to a phosphoryl groupsubstituted with at least one alkyl group, as defined herein; forexample, —P(O)(OH)Me.

The term “alkylthio” as used herein refers to alkyl-S—. The term“(alkylthio)alkyl” refers to an alkyl group substituted by an alkylthiogroup.

The term “carboxy”, as used herein, means a —CO₂H group.

The term “aryl” is a term of art and as used herein refers to includesmonocyclic, bicyclic and polycyclic aromatic hydrocarbon groups, forexample, benzene, naphthalene, anthracene, and pyrene. Typically, anaryl group contains from 6-10 carbon ring atoms (i.e., (C₆-C₁₀)aryl).The aromatic ring may be substituted at one or more ring positions withone or more substituents, such as halogen, azide, alkyl, aralkyl,alkenyl, alkynyl, cycloalkyl, hydroxyl, alkoxyl, amino, nitro,sulfhydryl, imino, amido, phosphonate, phosphinate, carbonyl, carboxyl,silyl, ether, alkylthio, sulfonyl, sulfonamido, ketone, aldehyde, ester,heterocyclyl, aromatic or heteroaromatic moieties, fluoroalkyl (such astrifluromethyl), cyano, or the like. The term “aryl” also includespolycyclic ring systems having two or more cyclic rings in which two ormore carbons are common to two adjoining rings (the rings are “fusedrings”) wherein at least one of the rings is an aromatic hydrocarbon,e.g., the other cyclic rings may be cycloalkyls, cycloalkenyls,cycloalkynyls, aryls, heteroaryls, and/or heterocyclyls. In certainembodiments, the term “aryl” refers to a phenyl group.

The term “heteroaryl” is a term of art and as used herein refers to amonocyclic, bicyclic, and polycyclic aromatic group having 3 to 12 totalatoms including one or more heteroatoms such as nitrogen, oxygen, orsulfur in the ring structure. Exemplary heteroaryl groups includeazaindolyl, benzo(b)thienyl, benzimidazolyl, benzofuranyl, benzoxazolyl,benzothiazolyl, benzothiadiazolyl, benzotriazolyl, benzoxadiazolyl,furanyl, imidazolyl, imidazopyridinyl, indolyl, indolinyl, indazolyl,isoindolinyl, isoxazolyl, isothiazolyl, isoquinolinyl, oxadiazolyl,oxazolyl, purinyl, pyranyl, pyrazinyl, pyrazolyl, pyridinyl,pyrimidinyl, pyrrolyl, pyrrolo[2,3-d]pyrimidinyl,pyrazolo[3,4-d]pyrimidinyl, quinolinyl, quinazolinyl, triazolyl,thiazolyl, thiophenyl, tetrahydroindolyl, tetrazolyl, thiadiazolyl,thienyl, thiomorpholinyl, triazolyl or tropanyl, and the like. The“heteroaryl” may be substituted at one or more ring positions with oneor more substituents such as halogen, azide, alkyl, aralkyl, alkenyl,alkynyl, cycloalkyl, hydroxyl, alkoxyl, amino, nitro, sulfhydryl, imino,amido, phosphonate, phosphinate, carbonyl, carboxyl, silyl, ether,alkylthio, sulfonyl, sulfonamido, ketone, aldehyde, ester, heterocyclyl,aromatic or heteroaromatic moieties, fluoroalkyl (such astrifluromethyl), cyano, or the like. The term “heteroaryl” also includespolycyclic ring systems having two or more cyclic rings in which two ormore carbons are common to two adjoining rings (the rings are “fusedrings”) wherein at least one of the rings is an aromatic group havingone or more heteroatoms in the ring structure, e.g., the other cyclicrings may be cycloalkyls, cycloalkenyls, cycloalkynyls, aryls,heteroaryls, and/or heterocyclyls.

The term “aralkyl” or “arylalkyl” is a term of art and as used hereinrefers to an alkyl group substituted with an aryl group, wherein themoiety is appended to the parent molecule through the alkyl group.

The term “heteroaralkyl” or “heteroarylalkyl” is a term of art and asused herein refers to an alkyl group substituted with a heteroarylgroup, appended to the parent molecular moiety through the alkyl group.

The term “alkoxy” as used herein means an alkyl group, as definedherein, appended to the parent molecular moiety through an oxygen atom.Representative examples of alkoxy include, but are not limited to,methoxy, ethoxy, propoxy, 2-propoxy, butoxy, tert-butoxy, pentyloxy, andhexyloxy.

The term “alkoxyalkyl” refers to an alkyl group substituted by an alkoxygroup.

The term “alkoxycarbonyl” means an alkoxy group, as defined herein,appended to the parent molecular moiety through a carbonyl group,represented by —C(═O)—, as defined herein. Representative examples ofalkoxycarbonyl include, but are not limited to, methoxycarbonyl,ethoxycarbonyl, and tert-butoxycarbonyl.

The term “alkylcarbonyl”, as used herein, means an alkyl group, asdefined herein, appended to the parent molecular moiety through acarbonyl group, as defined herein. Representative examples ofalkylcarbonyl include, but are not limited to, acetyl, 1-oxopropyl,2,2-dimethyl-1-oxopropyl, 1-oxobutyl, and 1-oxopentyl.

The term “arylcarbonyl”, as used herein, means an aryl group, as definedherein, appended to the parent molecular moiety through a carbonylgroup, as defined herein. Representative examples of arylcarbonylinclude, but are not limited to, benzoyl and (2-pyridinyl)carbonyl.

The term “alkylcarbonyloxy” and “arylcarbonyloxy”, as used herein, meansan alkylcarbonyl or arylcarbonyl group, as defined herein, appended tothe parent molecular moiety through an oxygen atom. Representativeexamples of alkylcarbonyloxy include, but are not limited to, acetyloxy,ethylcarbonyloxy, and tert-butylcarbonyloxy. Representative examples ofarylcarbonyloxy include, but are not limited to phenylcarbonyloxy.

The term “alkenoxy” or “alkenoxyl” means an alkenyl group, as definedherein, appended to the parent molecular moiety through an oxygen atom.Representative examples of alkenoxyl include, but are not limited to,2-propen-1-oxyl (i.e., CH₂═CH—CH₂—O—) and vinyloxy (i.e., CH₂═CH—O—).

The term “aryloxy” as used herein means an aryl group, as definedherein, appended to the parent molecular moiety through an oxygen atom.

The term “heteroaryloxy” as used herein means a heteroaryl group, asdefined herein, appended to the parent molecular moiety through anoxygen atom.

The term “carbocyclyl” as used herein means a monocyclic or multicyclic(e.g., bicyclic, tricyclic, etc.) hydrocarbon radical containing from 3to 12 carbon atoms that is completely saturated or has one or moreunsaturated bonds, and for the avoidance of doubt, the degree ofunsaturation does not result in an aromatic ring system (e.g., phenyl).Examples of carbocyclyl groups include 1-cyclopropyl, 1-cyclobutyl,2-cyclopentyl, 1-cyclopentenyl, 3-cyclohexyl, 1-cyclohexenyl and2-cyclopentenylmethyl.

The term “cyano” is a term of art and as used herein refers to CN.

The term “halo” is a term of art and as used herein refers to F, Cl,—Br, or I.

The term “haloalkyl” as used herein refers to an alkyl group, as definedherein, wherein some or all of the hydrogens are replaced with halogenatoms.

The term “hydroxy” is a term of art and as used herein refers to OH.

The term “hydroxyalkyl”, as used herein, means at least one hydroxygroup, as defined herein, is appended to the parent molecular moietythrough an alkyl group, as defined herein. Representative examples ofhydroxyalkyl include, but are not limited to, hydroxymethyl,2-hydroxyethyl, 3-hydroxypropyl, 2,3-dihydroxypentyl, and2-ethyl-4-hydroxyheptyl.

The term “silyl”, as used herein, includes hydrocarbyl derivatives ofthe silyl (H3Si—) group (i.e., (hydrocarbyl)₃Si), wherein a hydrocarbylgroups are univalent groups formed by removing a hydrogen atom from ahydrocarbon, e.g., ethyl, phenyl. The hydrocarbyl groups can becombinations of differing groups which can be varied in order to providea number of silyl groups, such as trimethylsilyl (TMS),tert-butyldiphenylsilyl (TBDPS), tert-butyldimethylsilyl (TBS/TBDMS),triisopropylsilyl (TIPS), and [2-(trimethylsilyl)ethoxy]methyl (SEM).

The term “silyloxy”, as used herein, means a silyl group, as definedherein, is appended to the parent molecule through an oxygen atom.

Certain compounds contained in compositions of the present invention mayexist in particular geometric or stereoisomeric forms. In addition,compounds of the present invention may also be optically active. Thepresent invention contemplates all such compounds, including cis- andtrans-isomers, (R)- and (S)-enantiomers, diastereoisomers, (D)-isomers,(L)-isomers, the racemic mixtures thereof, and other mixtures thereof,as falling within the scope of the invention. Additional asymmetriccarbon atoms may be present in a substituent such as an alkyl group. Allsuch isomers, as well as mixtures thereof, are intended to be includedin this invention.

If, for instance, a particular enantiomer of compound of the presentinvention is desired, it may be prepared by asymmetric synthesis, or byderivation with a chiral auxiliary, where the resulting diastereomericmixture is separated and the auxiliary group cleaved to provide the puredesired enantiomers. Alternatively, where the molecule contains a basicfunctional group, such as amino, or an acidic functional group, such ascarboxyl, diastereomeric salts are formed with an appropriateoptically-active acid or base, followed by resolution of thediastereomers thus formed by fractional crystallization orchromatographic means well known in the art, and subsequent recovery ofthe pure enantiomers.

It will be understood that “substitution” or “substituted with” includesthe implicit proviso that such substitution is in accordance withpermitted valence of the substituted atom and the substituent, and thatthe substitution results in a stable compound, e.g., which does notspontaneously undergo transformation such as by rearrangement,fragmentation, decomposition, cyclization, elimination, or otherreaction.

The term “substituted” is also contemplated to include all permissiblesubstituents of organic compounds. In a broad aspect, the permissiblesubstituents include acyclic and cyclic, branched and unbranched,carbocyclic and heterocyclic, aromatic and nonaromatic substituents oforganic compounds. Illustrative substituents include, for example, thosedescribed herein above. The permissible substituents may be one or moreand the same or different for appropriate organic compounds. Forpurposes of this invention, the heteroatoms such as nitrogen may havehydrogen substituents and/or any permissible substituents of organiccompounds described herein which satisfy the valences of theheteroatoms. This invention is not intended to be limited in any mannerby the permissible substituents of organic compounds.

The phrase “protecting group”, as used herein, means temporarysubstituents which protect a potentially reactive functional group fromundesired chemical transformations. Examples of such protecting groupsinclude esters of carboxylic acids, silyl ethers of alcohols, andacetals and ketals of aldehydes and ketones, respectively. The field ofprotecting group chemistry has been reviewed (Greene, T. W.; Wuts, P. G.M. Protective Groups in Organic Synthesis, 2nd ed.; Wiley: New York,1991). Protected forms of the inventive compounds are included withinthe scope of this invention.

For purposes of the invention, the chemical elements are identified inaccordance with the Periodic Table of the Elements, CAS version,Handbook of Chemistry and Physics, 67th Ed., 1986-87, inside cover.

Other chemistry terms herein are used according to conventional usage inthe art, as exemplified by The McGraw-Hill Dictionary of Chemical Terms(ed. Parker, S., 1985), McGraw-Hill, San Francisco, incorporated hereinby reference). Unless otherwise defined, all technical and scientificterms used herein have the same meaning as commonly understood by one ofordinary skill in the art to which this invention pertains.

The term “pharmaceutically acceptable salt” as used herein includessalts derived from inorganic or organic acids including, for example,hydrochloric, hydrobromic, sulfuric, nitric, perchloric, phosphoric,formic, acetic, lactic, maleic, fumaric, succinic, tartaric, glycolic,salicylic, citric, methanesulfonic, benzenesulfonic, benzoic, malonic,trifluoroacetic, trichloroacetic, naphthalene-2-sulfonic, and otheracids. Pharmaceutically acceptable salt forms can include forms whereinthe ratio of molecules comprising the salt is not 1:1. For example, thesalt may comprise more than one inorganic or organic acid molecule permolecule of base, such as two hydrochloric acid molecules per moleculeof compound of Formula I. As another example, the salt may comprise lessthan one inorganic or organic acid molecule per molecule of base, suchas two molecules of compound of Formula I per molecule of tartaric acid.

The terms “carrier” and “pharmaceutically acceptable carrier” as usedherein refer to a diluent, adjuvant, excipient, or vehicle with which acompound is administered or formulated for administration. Non-limitingexamples of such pharmaceutically acceptable carriers include liquids,such as water, saline, and oils; and solids, such as gum acacia,gelatin, starch paste, talc, keratin, colloidal silica, urea, and thelike. In addition, auxiliary, stabilizing, thickening, lubricating,flavoring, and coloring agents may be used. Other examples of suitablepharmaceutical carriers are described in Remington's PharmaceuticalSciences by E. W. Martin, herein incorporated by reference in itsentirety.

The term “treat” as used herein means prevent, halt or slow theprogression of, or eliminate a disease or condition in a subject. In oneembodiment “treat” means halt or slow the progression of, or eliminate adisease or condition in a subject. In one embodiment, “treat” meansreduce at least one objective manifestation of a disease or condition ina subject.

The term “effective amount” as used herein refers to an amount that issufficient to bring about a desired biological effect.

The term “therapeutically effective amount” as used herein refers to anamount that is sufficient to bring about a desired therapeutic effect.

The term “inhibit” as used herein means decrease by an objectivelymeasurable amount or extent. In various embodiments “inhibit” meansdecrease by at least 5, 10, 20, 30, 40, 50, 60, 70, 80, 90, or 95percent compared to relevant control. In one embodiment “inhibit” meansdecrease 100 percent, i.e., halt or eliminate.

The term “subject” as used herein refers to a mammal. In variousembodiments, a subject is a mouse, rat, rabbit, cat, dog, pig, sheep,horse, cow, or non-human primate. In one embodiment, a subject is ahuman.

Compounds

The present invention provides compounds of Formula (I), orpharmaceutically acceptable salts thereof:

-   wherein, independently for each occurrence:-   R¹ represents optionally substituted aryl, heteroaryl, cycloalkyl,    heterocycloalkyl, alkyl, or alkenyl;-   R² and R³ each independently represent H, F, or optionally    substituted alkyl, alkenyl, alkynyl, alkoxyalkyl, haloalkyl,    hydroxyalkyl, (alkylthio)alkyl, aralkyl, heteroaralkyl, cycloalkyl,    (cycloalkyl)alkyl, heterocycloalkyl, or (heterocycloalkyl)alkyl;-   or R² and R³, taken together with the carbon atom to which they are    bonded, form an optionally substituted cycloalkyl or    heterocycloalkyl ring;-   R⁴ represents H or optionally substituted alkyl, alkenyl, alkynyl,    cycloalkyl, (cycloalkyl)alkyl, heterocycloalkyl,    (heterocycloalkyl)alkyl, aralkyl, heteroaralkyl, hydroxyalkyl, or    haloalkyl;-   X represents NH, CH₂, CHF, CF₂, CH(C₁-C₆)alkyl, or C((C₁-C₆)alkyl)₂;-   Y is absent or represents CH₂, C(O), CR¹⁵R¹⁶, S(O)₂, or optionally    substituted (C₃-C₇)cycloalkylene, arylene, or heteroarylene;-   R^(a) represents H or optionally substituted (C₁-C₆)alkyl,    (heterocycloalkyl)alkyl, or (C₃-C₇)cycloalkyl;-   m is an integer from 1-6;-   n is 0 or 1;-   R¹⁵ and R¹⁶ are each independently selected from the group    consisting of H, hydroxy, halogen, —C(O)OR¹⁷, —OR¹⁷, —C(O)NR¹⁷R¹⁸,    —NR¹⁷R¹⁸, alkyl, hydroxyalkyl, haloalkyl, alkoxyalkyl, aryl,    aralkyl, heteroaryl, heteroaralkyl, cycloalkyl, (cycloalkyl)alkyl,    heterocycloalkyl, and (heterocycloalkyl)alkyl, wherein alkyl, aryl,    aralkyl, heteroaryl, heteroaralkyl, cycloalkyl, (cycloalkyl)alkyl,    heterocycloalkyl, and (heterocycloalkyl)alkyl are optionally    substituted with one or more substituents selected from the group    consisting of —CN, —OR¹⁷, —NR¹⁷R¹⁸, halo, and alkyl;-   or R¹⁵ and R¹⁶ may be taken together with the intervening atom to    form an optionally substituted carbocyclic or heterocyclic ring;-   R¹⁷ and R¹⁸ are each independently selected from the group    consisting of H, alkyl, haloalkyl, hydroxyalkyl, alkoxyalkyl, aryl,    aralkyl, heteroaryl, heteroaralkyl, cycloalkyl, (cycloalkyl)alkyl,    heterocycloalkyl, and (heterocycloalkyl)alkyl;-   or R¹⁷ and R¹⁸, when attached to the same atom, may be taken    together with the intervening atom to form an optionally substituted    heterocyclic ring;

represents

-   Z¹ and Z³ each independently represent C or N;-   Z² represents N, CH, or CF;-   Z⁴ represents N or CR⁸;-   Z⁵ represents N or CR⁵;-   Z⁶ represents N or CR⁶;-   Z⁷ represents N or CR⁹;-   Z⁸ and Z⁹ each independently represent N or CR¹⁹;-   R⁵ and R⁶ each independently represent H, halogen, —CN, —NO₂, —OR¹³,    —NR¹³R¹⁴, —C(O)R¹³, —C(O)OR¹³, —C(O)NR¹³R¹⁴, —OC(O)R¹³,    —NR¹³C(O)R¹⁴, —OC(O)NR¹³R¹⁴, —OC(O)OR¹³, —NR¹³C(O)OR¹⁴,    —NR¹³C(O)NR¹³R¹⁴, —OS(O)_(p)(R¹³), —NR¹³S(O)_(p)(R¹⁴), or optionally    substituted alkyl, alkenyl, alkynyl, haloalkyl, aralkyl,    heteroaralkyl, heteroaryl, aryl, cycloalkyl, (cycloalkyl)alkyl,    heterocycloalkyl, or (heterocycloalkyl)alkyl;-   L represents —H, —CNc, —C(O)R⁷, —CH(OH)R⁷, or —S(O)_(p)(alkyl);-   R⁷, independently for each occurrence, represents H, NH₂, CH₃, OH,    CF₃, CH₂OH, (C₁-C₆)alkyl, hydroxy(C₁-C₆)alkyl,    (C₁-C₆)alkoxy(C₁-C₆)alkyl, halo(C₁-C₆)alkyl, NH(C₁-C₆)alkyl,    N((C₁-C₆)alkyl)₂;-   R⁸ and R⁹ each independently represent H, halogen, —OR¹³, —NR¹³R¹⁴,    —C(O)R¹³, —C(O)OR¹³, —C(O)NR¹³R¹⁴, —OC(O)R¹³, —NR¹³C(O)R¹⁴,    —OC(O)NR¹³R¹⁴, —OC(O)OR¹³, —NR¹³C(O)OR¹⁴, —NR¹³C(O)NR¹³R¹⁴,    —OS(O)_(p)(R¹³), —NR¹³S(O)_(p)(R¹⁴), or optionally substituted    alkyl, alkenyl, alkynyl, haloalkyl, aralkyl, heteroaralkyl,    heteroaryl, or aryl;-   or R⁵ and R⁸, or R⁵ and R⁶, or R⁶ and R⁹ may be taken together with    the intervening atoms to form an optionally substituted heterocyclic    or carbocyclic ring;-   R¹³ and R¹⁴, independently for each occurrence, represent H or    optionally substituted alkyl, alkenyl, alkynyl, aryl, aralkyl,    heteroaryl, heteroaralkyl, cycloalkyl, (cycloalkyl)alkyl,    heterocycloalkyl, or (heterocycloalkyl)alkyl; or, when R¹³ and R¹⁴    are attached to the same atom, R¹³ and R¹⁴ taken together with the    atom may form an optionally substituted heterocyclic ring;-   R¹⁹, independently for each occurrence, represents H, F, CN,    —C(O)R⁷, —CH(OH)R⁷, or —S(O)_(p)(alkyl);-   J represents H or NH₂; and-   p is 0, 1, or 2;-   wherein, if Z¹ is N, or if

represents

then X represents CH₂.

In preferred embodiments, n is 1.

In certain embodiments, R¹ represents aryl or heteroaryl, optionallysubstituted by one or more substituents independently selected from thegroup consisting of halogen, —CN, alkoxy, haloalkoxy, alkyl, haloalkyl,alkenyl, dialkylamino, heterocycloalkyl, aryl, and heteroaryl.

In certain embodiments, R¹ represents aryl or heteroaryl, optionallysubstituted by one or more substituents independently selected from thegroup consisting of halogen, alkoxy, haloalkoxy, alkyl, haloalkyl,alkenyl, dialkylamino, aryl, and heteroaryl.

In embodiments in which R¹ represents aryl or heteroaryl substituted byone or more substituents including an aryl or heteroaryl substituent,the aryl or heteroaryl substituent may be further substituted by one ormore substituents selected from the group consisting of alkyl andhalogen.

In certain embodiments, R¹ represents aryl or heteroaryl, optionallysubstituted by one or more substituents independently selected from thegroup consisting of halogen, alkoxy, haloalkoxy, alkyl, haloalkyl,alkenyl, and dialkylamino.

In certain embodiments, R¹ represents aryl or heteroaryl, substituted byone or more substituents, at least one of which is halogen. For example,R¹ may represent phenyl, substituted by a chloro and a fluoro group.

In other embodiments, R¹ represents phenyl, pyridinyl, pyrazinyl, orpyrimidinyl, optionally substituted by one or more substituents selectedfrom the group consisting of halogen, alkoxy (e.g., methoxy), haloalkoxy(e.g., trifluoromethoxy), alkyl (e.g., methyl), haloalkyl (e.g.,trifluoromethyl), alkenyl (e.g., vinyl), and dialkylamino (e.g.,dimethylamino).

In alternative embodiments, R¹ is optionally substituted alkyl oralkenyl. For example, R¹ may be (C₁-C₆)alkyl or (C₂-C₆)alkenyl,optionally substituted by halogen, hydroxy, alkoxy, or haloalkoxy.

In other embodiments, R¹ is optionally substituted cycloalkyl orheterocycloalkyl. For example, R¹ may be cycloalkyl or heterocycloalkyl,optionally substituted by one or more substituents selected from thegroup consisting of halo, hydroxy, (C₁-C₆)alkyl, (C₁-C₆)alkoxy, andhalo(C₁-C₆)alkyl. In some embodiments, R¹ is a heterocycloalkyl that isfused at two adjacent positions to an aryl or heteroaryl ring (e.g., atetrahydroquinolinyl group).

In certain embodiments, R¹ is optionally substituted heteroaryl and Y isabsent; or, R¹ is optionally substituted aryl and Y is CH₂.

In certain embodiments, Y is absent or represents CH₂.

In certain embodiments, Y is absent. Alternatively, Y is CH₂.

Alternatively, Y can be optionally substituted (C₃-C₇)cycloalkylene. Forexample, Y can be cyclopropylene substituted by fluoro.

In other alternative embodiments, Y can be optionally substitutedarylene or heteroarylene. For example, Y can be phenylene orpyridinylene, optionally substituted by halo or alkyl.

In alternative embodiments, Y is CR¹⁵R¹⁶. In certain such embodiments,R¹⁵ and R¹⁶ are selected from the group consisting of H, alkyl,hydroxyalkyl, haloalkyl, alkoxyalkyl, aralkyl, heteroaralkyl,(cycloalkyl)alkyl, and (heterocycloalkyl)alkyl, wherein alkyl, aryl,aralkyl, heteroaryl, heteroaralkyl, cycloalkyl, (cycloalkyl)alkyl,heterocycloalkyl, and (heterocycloalkyl)alkyl are optionally substitutedwith one or more substituents selected from the group consisting of —CN,—OR¹⁷, —NR¹⁷R¹⁸, halo, and alkyl, and further wherein R¹⁷ and R¹⁸ areeach independently selected from the group consisting of H and alkyl.

Alternatively, Y is CR¹⁵R¹⁶ and R¹⁵ and R¹⁶ are taken together with theintervening atom to form an optionally substituted carbocyclic orheterocyclic ring, e.g., a cyclopropyl ring.

In certain embodiments, Y represents CH(C₁-C₆)alkyl. Alternatively, Yrepresents CH(C₁-C₆)alkyl, wherein the (C₁-C₆)alkyl is substituted byhydroxy, alkoxy, or di(alkyl)amino.

In certain embodiments, R² and R³ each independently represent H oroptionally substituted alkyl, alkenyl, alkynyl, alkoxyalkyl, haloalkyl,hydroxyalkyl, (alkylthio)alkyl, aralkyl, heteroaralkyl, cycloalkyl,(cycloalkyl)alkyl, heterocycloalkyl, or (heterocycloalkyl)alkyl.

In certain embodiments, R² is H and R³ represents H or optionallysubstituted alkyl, alkoxyalkyl, hydroxyalkyl, (alkylthio)alkyl, aralkyl,heteroaralkyl, cycloalkyl, or (cycloalkyl)alkyl.

In certain embodiments, both R² and R³ represent H.

Alternatively, both R² and R³ may represent alkyl, e.g., methyl.

In further embodiments, R² and R³, taken together with the interveningatom, form an optionally substituted carbocyclic or heterocyclic ring.

In certain embodiments, R⁴ represents H or optionally substituted alkyl,cycloalkyl, (cycloalkyl)alkyl, heterocycloalkyl, aralkyl, hydroxyalkyl,or haloalkyl; preferably R⁴ represents H or optionally substituted alkylor cycloalkyl.

In certain embodiments, R⁴ represents H or alkyl, alkenyl, alkynyl,cycloalkyl, (cycloalkyl)alkyl, heterocycloalkyl,(heterocycloalkyl)alkyl, aralkyl, heteroaralkyl, hydroxyalkyl, orhaloalkyl, each optionally substituted by one or more substituentsindependently selected from the group consisting of halo, alkoxy, alkyl,hydroxy, hydroxyalkyl, haloalkyl, NH₂, —NH(alkyl), —N(alkyl)₂,—C(O)O(alkyl), —C(O)NH₂, —S(O)₂(alkyl), —NHS(O)₂(alkyl), and—NHC(O)(O(alkyl)).

In exemplary embodiments, R⁴ represents

In certain embodiments, R^(a) represents (C₁-C₆)alkyl,(heterocycloalkyl)alkyl, or (C₃-C₇)cycloalkyl, optionally substituted byhydroxy or dialkylamino.

In certain embodiments, R^(a) represents H, (C₁-C₆)alkyl, or(C₃-C₇)cycloalkyl. In further embodiments, R^(a) represents H.Alternatively, in some embodiments, R^(a) represents (C₁-C₆)alkyl.

In certain embodiments, m is an integer from 1-4. In some embodiments, mis 1 or 2. Preferably, m is 1.

In certain embodiments,

represents

Alternatively,

represents

In further embodiments,

represents

In some embodiments,

may represent

wherein R⁸, L, and Z² are as defined above. For example,

may represent

In certain such embodiments, R⁸ is preferably H, NH₂, or Cl. In furthersuch embodiments, L represents H or CN.

In certain embodiments, L represents C(O)R⁷.

In certain embodiments, the compound of Formula (I) has the structure ofFormula (Ia):

In certain embodiments, the compound of Formula (I) has the structure ofFormula (Ib):

In certain embodiments, the compound of Formula (I) has the structure ofFormula (Ic):

In certain embodiments, the compound of Formula (I) has the structure ofFormula (Id):

In certain embodiments of the compounds of formulae (Ic) or (Id), X isNH.

In certain embodiments of the compounds of formula (I), if Z¹ is N, thenX is CH₂. In further embodiments, Z¹ is C, then X is NH.

In certain embodiments of the compounds of formulae (Ia), (Ib), (Ic), or(Id), Z⁴ represents CR⁸, Z⁵ represents CR⁵, Z⁶ represents CR⁶, and Z⁷represents CR⁹.

In certain embodiments, Z⁴ and Z⁷ each represent CH.

In certain embodiments, Z⁵ represents CR⁵ and Z⁶ represents CR⁶; and

R⁵ and R⁶ each independently represent H, halogen, —NR¹³R¹⁴, —C(O)R¹³,—C(O)OR¹³, —C(O)NHR¹⁴, —NHC(O)NR¹³R¹⁴, —NHS(O)₂(R¹⁴), or optionallysubstituted alkyl, alkenyl, alkynyl, heteroaryl, or aryl.

In certain such embodiments, R¹³ and R¹⁴, independently for eachoccurrence, represent H or optionally substituted aryl, aralkyl,heteroaryl, heteroaralkyl, cycloalkyl, or (cycloalkyl)alkyl.

In further embodiments, R⁵ and R⁶ each independently represent H oralkyl, alkenyl, alkynyl, heteroaryl, or aryl, optionally substitutedwith one or more substituents selected from the group consisting ofaryl, heteroaryl, silyl, alkyl, amino, alkylamino, dialkylamino,—C(O)(alkyl), heterocycloalkyl, and halogen. Alternatively, R⁵ and R⁶each independently represent H or alkyl, alkenyl, alkynyl, heteroaryl,or aryl, optionally substituted with one or more substituents selectedfrom the group consisting of aryl, heteroaryl, silyl, alkyl, amino,alkylamino, dialkylamino, —C(O)(alkyl), and halogen.

In certain embodiments, R¹³ and R¹⁴, independently for each occurrence,represent H or alkyl, alkenyl, alkynyl, aryl, aralkyl, heteroaryl,heteroaralkyl, cycloalkyl, (cycloalkyl)alkyl, heterocycloalkyl, or(heterocycloalkyl)alkyl, optionally substituted by one or moresubstituents independently selected from halo, alkoxy, alkyl, hydroxy,hydroxyalkyl, haloalkyl, —NH₂, —NH(alkyl), —N(alkyl)₂, —C(O)O(alkyl),—C(O)NH₂, —S(O)₂(alkyl), —NHS(O)₂(alkyl), and —NHC(O)(O(alkyl)).

In certain embodiments, R⁵ and R⁶ each independently represent H,halogen, —OR¹³, —NR¹³R¹⁴, —C(O)R¹³, —C(O)OR¹³, —C(O)NR¹³R¹⁴, —OC(O)R¹³,—NR¹³C(O)R¹⁴, —OC(O)NR¹³R¹⁴, —OC(O)OR¹³, —NR¹³C(O)OR¹⁴,—NR¹³C(O)NR¹³R¹⁴c, —OS(O)_(p)(R¹³), —NR¹³S(O)_(p)(R¹⁴), or optionallysubstituted alkyl, alkenyl, alkynyl, haloalkyl, aralkyl, heteroaralkyl,heteroaryl, aryl, cycloalkyl, (cycloalkyl)alkyl, heterocycloalkyl, or(heterocycloalkyl)alkyl.

In certain embodiments, R⁵, R⁶, R⁸, and R⁹ each independently representH or alkyl, alkenyl, alkynyl, haloalkyl, aralkyl, heteroaralkyl,heteroaryl, aryl, cycloalkyl, (cycloalkyl)alkyl, heterocycloalkyl, or(heterocycloalkyl)alkyl, optionally substituted with one or moresubstituents selected from the group consisting of aryl, heteroaryl,silyl, alkyl, amino, alkylamino, dialkylamino, —C(O)(alkyl), hydroxy,alkoxy, aryloxy, heteroaryloxy, and halogen.

In certain embodiments, R⁵, R⁶, R⁸, and R⁹ each independently representH or alkyl, alkenyl, alkynyl, heteroaryl, or aryl, optionallysubstituted with one or more substituents selected from the groupconsisting of aryl, heteroaryl, silyl, alkyl, amino, alkylamino,dialkylamino, —C(O)(alkyl), hydroxy, alkoxy, aryloxy, heteroaryloxy, andhalogen.

In certain embodiments, R⁵, R⁶, R⁸, and R⁹ each independently representH or —CH(OH)R⁵⁰, —CH(NH₂)R⁵⁰, —CH(OR⁵¹)R⁵⁰, —CH(NHR⁵¹)R⁵⁰,—C(NH₂)(R⁵¹)(R⁵⁰), —C(OH)(R⁵¹)(R⁵⁰), and —NH(CO)CR⁵R⁶R⁵⁰; wherein foreach occurrence R⁵⁰ and R⁵¹ are each independently selected from alkyl,alkenyl, alkynyl, haloalkyl, aralkyl, heteroaralkyl, heteroaryl, aryl,cycloalkyl, (cycloalkyl)alkyl, heterocycloalkyl, and(heterocycloalkyl)alkyl.

In certain embodiments, R⁵, R⁶, and R⁸ are each H.

In certain embodiments, R⁵, R⁶, and R⁹ are each H.

In certain embodiments, R⁵, R⁸, and R⁹ are each H.

In certain embodiments, R⁶, R⁸, and R⁹ are each H.

In certain embodiments, R⁷ represents NH₂, CH₃, or CF₃.

In certain embodiments, R⁷ represents NH₂.

In certain embodiments, the compound of the invention is selected fromthe group consisting of the following table of compounds, or apharmaceutically acceptable salt thereof:

Pharmaceutical Compositions

The invention provides pharmaceutical compositions, each comprising oneor more compounds of the invention and a pharmaceutically acceptablecarrier. In certain embodiments, the pharmaceutical compositioncomprises a compound of the invention and a pharmaceutically acceptablecarrier. In certain embodiments, the pharmaceutical compositioncomprises a plurality of compounds of the invention and apharmaceutically acceptable carrier.

In certain embodiments, a pharmaceutical composition of the inventionfurther comprises at least one additional pharmaceutically active agentother than a compound of the invention. The at least one additionalpharmaceutically active agent can be an agent useful in the treatment ofa disease or condition characterized by aberrant complement systemactivity.

Pharmaceutical compositions of the invention can be prepared bycombining one or more compounds of the invention with a pharmaceuticallyacceptable carrier and, optionally, one or more additionalpharmaceutically active agents.

Methods of Use

The present invention provides compounds that useful for treating orpreventing a disease or condition characterized by aberrant complementsystem activity.

In certain aspects, the invention provides a compound of the invention,or a pharmaceutically acceptable salt thereof, for use as a medicament.

In certain aspects, the invention provides methods of treating orpreventing a disease or condition characterized by aberrant complementsystem activity. The method includes the step of administering to asubject in need thereof a therapeutically effective amount of a compoundof the invention, or a pharmaceutically acceptable salt thereof, therebytreating or preventing the disease or condition characterized byaberrant complement system activity. By reducing complement systemactivity in the subject, the disease or condition characterized byaberrant complement system activity is treated.

Alternatively, in certain aspects, the invention provides a compound ofthe invention, or a pharmaceutically acceptable salt thereof, fortreatment of a disease or condition characterized by aberrant complementsystem activity.

Alternatively, in certain aspects, the invention provides the use of acompound of the invention, or a pharmaceutically acceptable saltthereof, for the manufacture of a medicament for use in treatment of adisease or condition characterized by aberrant complement systemactivity.

As used herein, a “disease or condition characterized by aberrantcomplement system activity” refers to any disease or condition in whichit is desirable to reduce complement system activity. For example, itmay be desirable to reduce complement system activity in the setting ofinappropriate activation or hyperactivation of the complement system.

In certain embodiments, the disease or condition characterized byaberrant complement system activity is an immunological disorder.

In certain embodiments, the disease or condition characterized byaberrant complement system activity is a disease of the central nervoussystem.

In certain embodiments, the disease or condition characterized byaberrant complement system activity is a renal disease.

In certain embodiments, the disease or condition characterized byaberrant complement system activity is a cardiovascular disease.

In certain embodiments, the disease or condition characterized byaberrant complement system activity is a neurodegenerative disease orneurological disease

In certain embodiments, the disease or condition characterized byaberrant complement system activity is selected from the groupconsisting of paroxysmal nocturnal hemoglobinuria, atypical hemolyticuremic syndrome, organ transplant rejection, myasthenia gravis,neuromyelitis optica, membranoproliferative glomerulonephritis,dense-deposit disease, cold agglutinin disease, and catastrophicantiphospholipid syndrome.

In certain embodiments, the disease or condition is paroxysmal nocturnalhemoglobinuria.

In certain embodiments, the disease or condition is atypical hemolyticuremic syndrome.

In certain embodiments, the disease or condition is organ transplantrejection.

In certain embodiments, the disease or condition is myasthenia gravis.

In certain embodiments, the disease or condition is neuromyelitisoptica.

In certain embodiments, the disease or condition ismembranoproliferative glomerulonephritis.

In certain embodiments, the disease or condition is dense-depositdisease.

In certain embodiments, the disease or condition is cold agglutinindisease.

In certain embodiments, the disease or condition is catastrophicantiphospholipid syndrome.

In other embodiments, the the disease or condition characterized byaberrant complement system activity is adult respiratory distresssyndrome, myocardial infarct, lung inflammation, hyperacute rejection(transplantation rejection), sepsis, cardiopulmonary bypass, burns,asthma, restenosis, multiple organ dysfunction syndrome, Guillain-Barrésyndrome, hemorrhagic shock, paroxysmal nocturnal hemoglobinuria,glomerulonephritis, systemic lupus erythematosus, rheumatoid arthritis,infertility, Alzheimer's disease, organ rejection (transplantation),myasthenia gravis, multiple sclerosis, platelet storage, orhemodialysis.

Formulations, Routes of Administration, and Dosing

The compounds of the invention can be formulated as pharmaceuticalcompositions and administered to a mammalian host, such as a humanpatient, in a variety of forms adapted to the chosen route ofadministration, e.g., orally or parenterally, by intravenous,intraperitoneal, intramuscular, topical, or subcutaneous routes.Additional routes of administration are also contemplated by theinvention.

Thus, the present compounds may be systemically administered, e.g.,orally, in combination with a pharmaceutically acceptable vehicle suchas an inert diluent or an assimilable edible carrier. They may beenclosed in hard or soft shell gelatin capsules, may be compressed intotablets, or may be incorporated directly with the food of the patient'sdiet. For oral therapeutic administration, the active compound may becombined with one or more excipients and used in the form of ingestibletablets, buccal tablets, troches, capsules, elixirs, suspensions,syrups, wafers, and the like. Such compositions and preparations shouldcontain at least 0.1% of active compound. The percentage of thecompositions and preparations may, of course, be varied and mayconveniently be between about 2% to about 60% of the weight of a givenunit dosage form. The amount of active compound in such therapeuticallyuseful compositions is such that an effective dosage level will beobtained.

The tablets, troches, pills, capsules, and the like may also contain thefollowing diluents and carriers: binders such as gum tragacanth, acacia,corn starch or gelatin; excipients such as dicalcium phosphate; adisintegrating agent such as corn starch, potato starch, alginic acidand the like; a lubricant such as magnesium stearate; and a sweeteningagent such as sucrose, fructose, lactose or aspartame or a flavoringagent such as peppermint, oil of wintergreen, or cherry flavoring may beadded. When the unit dosage form is a capsule, it may contain, inaddition to materials of the above type, a liquid carrier, such as avegetable oil or a polyethylene glycol. Various other materials may bepresent as coatings or to otherwise modify the physical form of thesolid unit dosage form. For instance, tablets, pills, or capsules may becoated with gelatin, wax, shellac or sugar and the like. A syrup orelixir may contain the active compound, sucrose or fructose as asweetening agent, methyl and propylparabens as preservatives, a dye andflavoring such as cherry or orange flavor. Of course, any material usedin preparing any unit dosage form should be pharmaceutically acceptableand substantially non-toxic in the amounts employed. In addition, theactive compound may be incorporated into sustained-release preparationsand devices.

The active compound may also be administered intravenously orintraperitoneally by infusion or injection. Solutions of the activecompound or its salts can be prepared in water or physiologicallyacceptable aqueous solution, optionally mixed with a nontoxicsurfactant. Dispersions can also be prepared in glycerol, liquidpolyethylene glycols, triacetin, and mixtures thereof and in oils. Underordinary conditions of storage and use, these preparations contain apreservative to prevent the growth of microorganisms.

The pharmaceutical dosage forms suitable for injection or infusion caninclude sterile aqueous solutions or dispersions or sterile powderscomprising the active ingredient which are adapted for theextemporaneous preparation of sterile injectable or infusible solutionsor dispersions, optionally encapsulated in liposomes. In all cases, theultimate dosage form should be sterile, fluid and stable under theconditions of manufacture and storage. The liquid carrier or vehicle canbe a solvent or liquid dispersion medium comprising, for example, water,ethanol, a polyol (for example, glycerol, propylene glycol, liquidpolyethylene glycols, and the like), vegetable oils, nontoxic glycerylesters, and suitable mixtures thereof. The proper fluidity can bemaintained, for example, by the formation of liposomes, by themaintenance of the required particle size in the case of dispersions orby the use of surfactants. The prevention of the action ofmicroorganisms can be brought about by various antibacterial andantifungal agents, for example, parabens, chlorobutanol, phenol, sorbicacid, thimerosal, and the like. In many cases, it will be preferable toinclude isotonic agents, for example, sugars, buffers or sodiumchloride. Prolonged absorption of the injectable compositions can bebrought about by the use in the compositions of agents delayingabsorption, for example, aluminum monostearate and gelatin.

Sterile injectable solutions are prepared by incorporating the activecompound in the required amount in the appropriate solvent with variousof the other ingredients enumerated above, as required, followed byfilter sterilization. In the case of sterile powders for the preparationof sterile injectable solutions, methods of preparation can includevacuum drying and the freeze drying techniques, which yield a powder ofthe active ingredient plus any additional desired ingredient present inthe previously sterile-filtered solutions.

For topical administration, the present compounds may be applied in pureform, i.e., when they are liquids. However, it will generally bedesirable to administer them to the skin as compositions orformulations, in combination with a dermatologically acceptable carrier,which may be a solid or a liquid.

Useful solid carriers include finely divided solids such as talc, clay,microcrystalline cellulose, silica, alumina and the like. Useful liquidcarriers include water, alcohols or glycols or water-alcohol/glycolblends, in which the present compounds can be dissolved or dispersed ateffective levels, optionally with the aid of non-toxic surfactants.Adjuvants such as fragrances and additional antimicrobial agents can beadded to optimize the properties for a given use. The resultant liquidcompositions can be applied from absorbent pads, used to impregnatebandages and other dressings, or sprayed onto the affected area usingpump-type or aerosol sprayers.

Thickeners such as synthetic polymers, fatty acids, fatty acid salts andesters, fatty alcohols, modified celluloses or modified mineralmaterials can also be employed with liquid carriers to form spreadablepastes, gels, ointments, soaps, and the like, for application directlyto the skin of the user.

Examples of useful dermatological compositions which can be used todeliver the compounds of the invention to the skin are known in the art;for example, see Jacquet et al. (U.S. Pat. No. 4,608,392; incorporatedherein by reference), Geria (U.S. Pat. No. 4,992,478; incorporatedherein by reference), Smith et al. (U.S. Pat. No. 4,559,157;incorporated herein by reference), and Wortzman (U.S. Pat. No.4,820,508; incorporated herein by reference).

Useful dosages of the compounds of the invention can be determined, atleast initially, by comparing their in vitro activity and in vivoactivity in animal models. Methods for the extrapolation of effectivedosages in mice, and other animals, to humans are known in the art; forexample, see U.S. Pat. No. 4,938,949 (incorporated herein by reference).

The amount of the compound, or an active salt thereof, required for usein treatment will vary not only with the particular compound or saltselected but also with the route of administration, the nature of thecondition being treated, and the age and condition of the patient andwill be ultimately at the discretion of the attendant physician orclinician.

In general, however, a suitable dose will be in the range of from about0.5 to about 100 mg/kg body weight of the recipient per day, e.g., fromabout 3 to about 90 mg/kg of body weight per day, from about 6 to about75 mg per kilogram of body weight per day, from about of 10 to about 60mg/kg of body weight per day, or from about 15 to about 50 mg/kg of bodyweight per day.

Compounds of the invention can be conveniently formulated in unit dosageform; for example, containing 5 to 1000 mg, 10 to 750 mg, or 50 to 500mg of active ingredient per unit dosage form. In one embodiment, theinvention provides a composition comprising a compound of the inventionformulated in such a unit dosage form. The desired dose may convenientlybe presented in a single dose or as divided doses to be administered atappropriate intervals, for example, as two, three, four or moresub-doses per day. The sub-dose itself may be further divided, e.g.,into a number of discrete loosely spaced administrations.

Compounds of the invention can also be administered in combination withother therapeutic agents, for example, other agents that are useful fortreating or preventing ischemia, blood loss, or reperfusion injury.

Other delivery systems can include time-release, delayed release, orsustained release delivery systems such as are well-known in the art.Such systems can avoid repeated administrations of the active compound,increasing convenience to the subject and the physician. Many types ofrelease delivery systems are available and known to those of ordinaryskill in the art. Use of a long-term sustained release implant may bedesirable. Long-term release, as used herein, means that the deliverysystem or is implant constructed and arranged to deliver therapeuticlevels of the active ingredient for at least 30 days, and preferably 60days.

In certain embodiments, a compound of the invention is formulated forintraocular administration, for example direct injection or insertionwithin or in association with an intraocular medical device.

The compounds of the invention may be formulated for depositing into amedical device, which may include any of a variety of conventionalgrafts, stents, including stent grafts, catheters, balloons, baskets, orother device that can be deployed or permanently implanted within a bodylumen. As a particular example, it would be desirable to have devicesand methods which can deliver compounds of the invention to the regionof a body which has been treated by interventional technique.

In exemplary embodiment, a compound of the invention may be depositedwithin a medical device, such as a stent, and delivered to the treatmentsite for treatment of a portion of the body.

Stents have been used as delivery vehicles for therapeutic agents (i.e.,drugs). Intravascular stents are generally permanently implanted incoronary or peripheral vessels. Stent designs include those of U.S. Pat.No. 4,733,655 (Palmaz), U.S. Pat. No. 4,800,882 (Gianturco), or U.S.Pat. No. 4,886,062 (Wiktor). Such designs include both metal andpolymeric stents, as well as self-expanding and balloon-expandablestents. Stents may also be used to deliver a drug at the site of contactwith the vasculature, as disclosed in U.S. Pat. No. 5,102,417 (Palmaz),U.S. Pat. No. 5,419,760 (Narciso, Jr.), U.S. Pat. No. 5,429,634(Narciso, Jr.), and in International Patent Application Nos. WO 91/12779(Medtronic, Inc.) and WO 90/13332 (Cedars-Sanai Medical Center), forexample.

The term “deposited” means that the compound is coated, adsorbed,placed, or otherwise incorporated into the device by methods known inthe art. For example, the compound may be embedded and released fromwithin (“matrix type”) or surrounded by and released through (“reservoirtype”) polymer materials that coat or span the medical device. In thelatter example, the compound may be entrapped within the polymermaterials or coupled to the polymer materials using one or more thetechniques for generating such materials known in the art. In otherformulations, the compound may be linked to the surface of the medicaldevice without the need for a coating, for example by means ofdetachable bonds, and release with time or can be removed by activemechanical or chemical processes. In other formulations, the compoundmay be in a permanently immobilized form that presents the compound atthe implantation site.

In certain embodiments, the compound may be incorporated with polymercompositions during the formation of biocompatible coatings for medicaldevices, such as stents. The coatings produced from these components aretypically homogeneous and are useful for coating a number of devicesdesigned for implantation.

The polymer may be either a biostable or a bioabsorbable polymerdepending on the desired rate of release or the desired degree ofpolymer stability, but frequently a bioabsorbable polymer is preferredfor this embodiment since, unlike a biostable polymer, it will not bepresent long after implantation to cause any adverse, chronic localresponse. Bioabsorbable polymers that could be used include, but are notlimited to, poly(L-lactic acid), polycaprolactone, polyglycolide (PGA),poly(lactide-co-glycolide) (PLLA/PGA), poly(hydroxybutyrate),poly(hydroxybutyrate-co-valerate), polydioxanone, polyorthoester,polyanhydride, poly(glycolic acid), poly(D-lactic acid), poly(L-lacticacid), poly(D, L-lactic acid), poly(D, L-lactide) (PLA), poly(L-lactide) (PLLA), poly(glycolic acid-co-trimethylene carbonate)(PGA/PTMC), polyethylene oxide (PEO), polydioxanone (PDS),polyphosphoester, polyphosphoester urethane, poly(amino acids),cyanoacrylates, poly(trimethylene carbonate), poly(iminocarbonate),copoly(ether-esters) (e.g., PEO/PLA), polyalkylene oxalates,polyphosphazenes and biomolecules such as fibrin, fibrinogen, cellulose,starch, collagen and hyaluronic acid, polyepsilon caprolactone,polyhydroxy butyric acid, polyorthoesters, polyacetals,polydihydropyrans, polycyanoacrylates, cross linked or amphipathic blockcopolymers of hydrogels, and other suitable bioabsorbable poplymersknown in the art. Also, biostable polymers with a relatively low chronictissue response such as polyurethanes, silicones, and polyesters couldbe used, and other polymers could also be used if they can be dissolvedand cured or polymerized on the medical device such as polyolefins,polyisobutylene and ethylene-alphaolefin copolymers; acrylic polymersand copolymers, vinyl halide polymers and copolymers, such as polyvinylchloride; polyvinylpyrrolidone; polyvinyl ethers, such as polyvinylmethyl ether; polyvinylidene halides, such as polyvinylidene fluorideand polyvinylidene chloride; polyacrylonitrile, polyvinyl ketones;polyvinyl aromatics, such as polystyrene, polyvinyl esters, such aspolyvinyl acetate; copolymers of vinyl monomers with each other andolefins, such as ethylene-methyl methacrylate copolymers,acrylonitrile-styrene copolymers, ABS resins, and ethylene-vinyl acetatecopolymers; pyran copolymer; polyhydroxy-propyl-methacrylamide-phenol;polyhydroxyethyl-aspartamide-phenol; polyethyleneoxide-polylysinesubstituted with palmitoyl residues; polyamides, such as Nylon 66 andpolycaprolactam; alkyd resins, polycarbonates; polyoxymethylenes;polyimides; polyethers; epoxy resins, polyurethanes; rayon;rayon-triacetate; cellulose, cellulose acetate, cellulose butyrate;cellulose acetate butyrate; cellophane; cellulose nitrate; cellulosepropionate; cellulose ethers; and carboxymethyl cellulose.

Polymers and semipermeable polymer matrices may be formed into shapedarticles, such as valves, stents, tubing, prostheses and the like.

In certain embodiments of the invention, the compound of the inventionis coupled to a polymer or semipermeable polymer matrix that is formedas a stent or stent-graft device.

Typically, polymers are applied to the surface of an implantable deviceby spin coating, dipping, or spraying. Additional methods known in theart can also be utilized for this purpose. Methods of spraying includetraditional methods as well as microdeposition techniques with an inkjettype of dispenser. Additionally, a polymer can be deposited on animplantable device using photo-patterning to place the polymer on onlyspecific portions of the device. This coating of the device provides auniform layer around the device which allows for improved diffusion ofvarious analytes through the device coating.

In certain embodiments of the invention, the compound is formulated forrelease from the polymer coating into the environment in which themedical device is placed. Preferably, the compound is released in acontrolled manner over an extended time frame (e.g., months) using atleast one of several well-known techniques involving polymer carriers orlayers to control elution. Some of these techniques are described inU.S. Patent Application 2004/0243225A1, the entire disclosure of whichis incorporated herein in its entirety.

Moreover, as described for example in U.S. Pat. No. 6,770,729, which isincorporated herein in its entirety, the reagents and reactionconditions of the polymer compositions can be manipulated so that therelease of the compound from the polymer coating can be controlled. Forexample, the diffusion coefficient of the one or more polymer coatingscan be modulated to control the release of the compound from the polymercoating. In a variation on this theme, the diffusion coefficient of theone or more polymer coatings can be controlled to modulate the abilityof an analyte that is present in the environment in which the medicaldevice is placed (e.g., an analyte that facilitates the breakdown orhydrolysis of some portion of the polymer) to access one or morecomponents within the polymer composition (and for example, therebymodulate the release of the compound from the polymer coating). Yetanother embodiment of the invention includes a device having a pluralityof polymer coatings, each having a plurality of diffusion coefficients.In such embodiments of the invention, the release of the compound fromthe polymer coating can be modulated by the plurality of polymercoatings.

In yet another embodiment of the invention, the release of the compoundfrom the polymer coating is controlled by modulating one or more of theproperties of the polymer composition, such as the presence of one ormore endogenous or exogenous compounds, or alternatively, the pH of thepolymer composition. For example, certain polymer compositions can bedesigned to release a compound in response to a decrease in the pH ofthe polymer composition.

Kits

The invention also provides a kit, comprising a compound of theinvention, or a pharmaceutically acceptable salt thereof, at least oneother therapeutic agent, packaging material, and instructions foradministering the compound of the invention or the pharmaceuticallyacceptable salt thereof and the other therapeutic agent or agents to amammal to treat or prevent a disease or condition characterized byaberrant complement system activity. In one embodiment, the mammal is ahuman.

It will be understood by one of ordinary skill in the relevant arts thatother suitable modifications and adaptations to the compositions andmethods described herein are readily apparent from the description ofthe invention contained herein in view of information known to theordinarily skilled artisan, and may be made without departing from thescope of the invention or any embodiment thereof.

EXAMPLES

Having now described the present invention in detail, the same will bemore clearly understood by reference to the following examples, whichare included herewith for purposes of illustration only and are notintended to be limiting of the invention.

Scheme 1 depicts general synthesis of compounds of type (1f) and/or(1g). These compounds were prepared in a manner wherein (1a) or (1b)consisting of an activated carbonyl compound bearing a leaving group(Lv) upon reacting with free or protected amine under couplingconditions yields (1c). The compound (1d) was prepared by reaction offree or protected amine with (1c); the protecting group was removedusing standard conditions to form (1e). In the final step, compound (1e)was coupled with activated carbonyl group using a coupling reagent toform amide compounds (1f), subsequently substituted urea compounds (1g)were prepared from (1e) using structurally diverse isocyanate.

Preparation of(S)-1-(2-((1-((6-bromopyridin-2-yl)amino)-3-methyl-1-oxobutan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(2f) Step-1: Preparation of (S)-tert-butyl(1-((6-bromopyridin-2-yl)amino)-3-methyl-1-oxobutan-2-yl)carbamate (2c)

To a solution of Boc-L-valine (2a) (1.32 g, 6.07 mmol) and6-bromopyridin-2-amine (2b) (1.0 g, 5.78 mmol) in THF (20 mL) was addedethyl 2-ethoxyquinoline-1(2H)-carboxylate (EEDQ, 1.43 g, 5.78 mmol). Theresulting mixture was refluxed for 4 days, cooled to room temperature,diluted with EtOAc (100 mL), washed with KHSO₄ (1 N, 2×30 mL) and brine(20 mL). The organic layer was dried, concentrated in vacuum and theresidue obtained was purified by flash column chromatography [silica gel(12 g), eluting with EtOAc (0-50%) in hexane] to afford (S)-tert-butyl1-(6-bromopyridin-2-ylamino)-3-methyl-1-oxobutan-2-ylcarbamate (2c) (121mg, 0.325 mmol, 6% yield) as a semi-solid; ¹H NMR (300 MHz, DMSO-d₆) δ10.78 (s, 1H), 8.09 (d, J=8.1 Hz, 1H), 7.73 (t, J=7.9 Hz, 1H), 7.34 (d,J=7.7 Hz, 1H), 6.98 (d, J=8.4 Hz, 1H), 4.06-3.94 (m, 1H), 2.05-1.92 (m,1H), 1.37 (s, 9H), 0.93-0.86 (m, 6H); MS (ES+): 394.4 (M+Na).

Step-2: Preparation of(S)-2-amino-N-(6-bromopyridin-2-yl)-3-methylbutanamide (2d)

To a stirred solution of (S)-tert-butyl1-(6-bromopyridin-2-ylamino)-3-methyl-1-oxobutan-2-ylcarbamate (2c) (120mg, 0.322 mmol) in DCM (10 mL) was added TFA (368 mg, 3.22 mmol) at roomtemperature and stirred for 16 h. The reaction mixture was concentratedin vacuum to remove DCM and excess TFA to furnish(S)-2-amino-N-(6-bromopyridin-2-yl)-3-methylbutanamide (2d) which wasused as such in the next step without further purification; MS (ES+):273.3 (M+1).

Step-3: Preparation of(S)-1-(2-((1-((6-bromopyridin-2-yl)amino)-3-methyl-1-oxobutan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(2f)

To the above TFA salt of(S)-2-amino-N-(6-bromopyridin-2-yl)-3-methylbutanamide (2d) (120 mg,0.441 mmol) in DMF (4 mL) was added2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e) (116 mg, 0.529 mmol,prepared according to procedure reported by Altmann, Eva et al; in PCTInt. Appl., WO 2012/093101), DIPEA (0.308 mL, 1.764 mmol), HATU (201 mg,0.529 mmol) and stirred at room temperature overnight. The reactionmixture was diluted with EtOAc (100 mL), washed with water (3×), brine,dried, filtered and concentrated in vacuum to dryness. The residueobtained was purified by flash column chromatography [silica gel (12 g)eluting with 0-60% EtOAc/MeOH (9:1) in hexane] to furnish(S)-1-(2-((1-((6-bromopyridin-2-yl)amino)-3-methyl-1-oxobutan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(2f) (38 mg, 18% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ11.01 (s, 1H), 8.57 (d, J=8.1 Hz, 1H), 8.13 (dd, J=21.3, 8.2 Hz, 2H),7.81-7.56 (m, 3H), 7.39 (dd, J=23.5, 7.5 Hz, 3H), 7.25 (t, J=7.5 Hz,1H), 5.41-5.23 (m, 2H), 4.46 (t, J=7.2 Hz, 1H), 2.15-2.00 (m, 1H),1.00-0.83 (m, 7H); MS (ES+): 496.4 (M+Na).

Preparation of(S)-1-(2-((1-((3-chlorophenyl)amino)-3-methyl-1-oxobutan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(3d) Step-1: Preparation of(S)-tert-butyl-(3-chlorophenylamino)-3-methyl-1-oxobutan-2-ylcarbamate(3b)

Reaction of Boc-L-valine (2a) (1.73 g, 7.84 mmol) with 3-chloroaniline(3a) (1.0 g, 7.84 mmol) according to the procedure reported in step-1 ofScheme 2 gave after workup and purification (S)-tert-butyl1-(3-chlorophenylamino)-3-methyl-1-oxobutan-2-ylcarbamate (3b) (1.72 g,5.26 mmol, 67% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ10.20 (s, 1H), 7.84 (s, 1H), 7.46 (d, J=8.0 Hz, 1H), 7.34 (t, J=8.0 Hz,1H), 7.11 (d, J=7.4 Hz, 1H), 6.99 (d, J=8.1 Hz, 1H), 3.89 (t, J=7.7 Hz,1H), 2.09-1.80 (m, 1H), 1.39 (s, 9H), 0.89 (d, J=6.4 Hz, 6H); MS (ES+):349.4 (M+Na).

Step-2: Preparation of (S)-2-amino-N-(3-chlorophenyl)-3-methylbutanamide(3c)

Reaction of (S)-tert-butyl1-(3-chlorophenylamino)-3-methyl-1-oxobutan-2-ylcarbamate (3b) (750 mg,2.30 mmol) with TFA (2.62 g, 22.95 mmol) according to the procedurereported in step-2 of Scheme 2 gave after workup and purification bychromatography [silica (12 g) eluting with EtOAc/MeOH (9:1) in hexanefrom 0 to 60%] (S)-2-amino-N-(3-chlorophenyl)-3-methylbutanamide (3c)(355 mg, 1.57 mmol, 68% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 7.86-7.78 (m, 1H), 7.49 (d, J=7.9 Hz, 1H), 7.39 (t, J=7.9 Hz,1H), 7.18 (d, J=7.8 Hz, 1H), 3.66 (d, J=5.6 Hz, 1H), 2.21-2.05 (m, 1H),0.97 (t, J=7.1 Hz, 6H); MS (ES+): 227.3 (M+1).

Step-3: Preparation of(5)-1-(2-((1-((3-chlorophenyl)amino)-3-methyl-1-oxobutan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(3d)

Reaction of (S)-2-amino-N-(3-chlorophenyl)-3-methylbutanamide (3c) (145mg, 0.64 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e)according to the procedure reported in step-3 of Scheme 2 gave afterworkup and purification by chromatography [silica (12 g), eluting with0-60% EtOAc/MeOH (9:1) in hexane](S)-1-(2-((1-((3-chlorophenyl)amino)-3-methyl-1-oxobutan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(3d) (50 mg, 0.117 mmol, 18% yield) as a yellow solid; ¹H NMR (300 MHz,DMSO-d₆) δ 10.38 (s, 1H), 8.69 (d, J=8.3 Hz, 1H), 8.18 (d, J=7.9 Hz,1H), 7.83 (s, 1H), 7.76-7.59 (m, 2H), 7.52-7.31 (m, 4H), 7.26 (t, J=7.2Hz, 1H), 7.13 (d, J=7.7 Hz, 1H), 5.43-5.22 (m, 2H), 4.33 (t, J=7.5 Hz,1H), 2.22-1.86 (m, 1H), 0.95 (t, J=6.5 Hz, 6H); MS (ES+): 450.4 (M+Na)

Preparation of(S)-1-(2-((1-((6-bromopyridin-2-yl)amino)-3-methyl-1-oxobutan-2-yl)(methyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(4d) Step-1: Preparation of(5)-tert-butyl(1-((6-bromopyridin-2-yl)amino)-3-methyl-1-oxobutan-2-yl)(methyl)carbamate(4b)

Reaction of (S)-2-(tert-butoxycarbonyl)methyl)amino)-3-methylbutanoicacid (4a) (500 mg, 2.16 mmol) with 6-bromopyridin-2-amine (2b) (374 mg,2.16 mmol) according to the procedure reported in step-1 of Scheme 2gave after workup and purification by chromatography on silica gel (12g) of (5)-tert-butyl(1-((6-bromopyridin-2-yl)amino)-3-methyl-1-oxobutan-2-yl)(methyl)carbamate(4b) (135 mg, 0.35 mmol, 16% yield) as a semi-solid; ¹H NMR (300 MHz,DMSO-d₆) δ 10.92 (s, 1H), 8.08 (d, J=8.1 Hz, 1H), 7.74 (t, J=7.9 Hz,1H), 7.36 (d, J=8.0 Hz, 1H), 2.85 (s, 3H), 2.75 (s, 1H), 2.21-2.07 (m,1H), 1.40 (s, 9H), 0.93-0.83 (m, 6H); MS (ES+): 410.4 (M+Na); (ES⁻),386.3 (M−1).

Step-2: Preparation of(S)—N-(6-bromopyridin-2-yl)-3-methyl-2-(methylamino)butanamide (4c)

Reaction of (5)-tert-butyl(1-((6-bromopyridin-2-yl)amino)-3-methyl-1-oxobutan-2-yl)(methyl)carbamate(4b) (125 mg, 0.32 mmol) with TFA (369 mg, 3.24 mmol) according to theprocedure reported in step-2 of Scheme 2 gave after workup(S)—N-(6-bromopyridin-2-yl)-3-methyl-2-(methylamino)butanamide (4c) as aTFA salt which was used as such in next step without furtherpurification; MS (ES+): 288.3 (M+1).

Step-3: Preparation of(S)-1-(2-((1-((6-bromopyridin-2-yl)amino)-3-methyl-1-oxobutan-2-yl)(methyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(4d)

Reaction of above TFA salt of(S)—N-(6-bromopyridin-2-yl)-3-methyl-2-(methylamino)butanamide (4c) (99mg, 0.247 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e)(65.1 mg, 0.297 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup and purification by chromatography [silica(12 g), eluting with 0-60% EtOAc/MeOH (9:1) in hexane](S)-1-(2-((1-((6-bromopyridin-2-yl)amino)-3-methyl-1-oxobutan-2-yl)(methyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(4d) (53 mg, 0.11 mmol, 44% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 10.92 (s, 1H), 8.25-8.02 (m, 2H), 7.87-7.65 (m, 1H),7.65-7.50 (m, 2H), 7.46-7.31 (m, 3H), 7.31-7.18 (m, 1H), 5.78-5.44 (m,2H), 4.84 (d, J=10.8 Hz, 1H), 3.27-2.88 (m, 3H), 2.44-2.09 (m, 1H),1.12-0.79 (m, 6H); MS (ES+): 488.4 (M+1).

Preparation of(S)-1-(2-((1-((6-bromopyridin-2-yl)amino)-1-oxopropan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(5d) Step-1: Preparation of (5)-tert-butyl(1-((6-bromopyridin-2-yl)amino)-1-oxopropan-2-yl)carbamate (5b)

Reaction of (S)-2-(tert-butoxycarbonylamino)propanoic acid (5a) (1.15 g,6.07 mmol) with 6-bromopyridin-2-amine (2b) (1.0 g, 5.78 mmol) accordingto the procedure reported in step-1 of Scheme 2 gave after workup andpurification by chromatography (5)-tert-butyl(1-((6-bromopyridin-2-yl)amino)-1-oxopropan-2-yl)carbamate (5b) (250 mg,0.73 mmol, 13% yield) as a clear oil; MS (ES−): 342.4 (M−1).

Step-2: Preparation of (S)-2-amino-N-(6-bromopyridin-2-yl)propanamide)(5c)

Reaction of (5)-tert-butyl(1-((6-bromopyridin-2-yl)amino)-1-oxopropan-2-yl)carbamate (5b) (225 mg,0.65 mmol) with TFA (745 mg, 6.54 mmol) according to the procedurereported in step-2 of Scheme 2 gave after workup(S)-2-amino-N-(6-bromopyridin-2-yl)propanamide) (5c) as TFA salt whichwas used in next step without further purification; MS (ES+): 245.2(M+1).

Step-3: Preparation of(S)-1-(2-((1-((6-bromopyridin-2-yl)amino)-1-oxopropan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(5d)

Reaction of above TFA salt of(S)-2-amino-N-(6-bromopyridin-2-yl)propanamide) (5c) (125 mg, 0.35 mmol)with 2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e) (92 mg, 0.419 mmol)according to the procedure reported in step-3 of Scheme 2 gave afterworkup and purification by chromatography [silica (12 g), eluting with0-60% EtOAc/MeOH (9:1) in hexane](S)-1-(2-((1-((6-bromopyridin-2-yl)amino)-1-oxopropan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(5d) (18 mg, 12% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ10.96 (s, 1H), 8.75 (d, J=6.9 Hz, 1H), 8.16 (d, J=8.2 Hz, 1H), 8.07 (d,J=8.2 Hz, 1H), 7.79-7.56 (m, 3H), 7.47-7.30 (m, 3H), 7.30-7.18 (m, 1H),5.26 (s, 2H), 4.71-4.36 (m, 1H), 1.34 (d, J=7.1 Hz, 3H); MS (ES+): 467.4(M+Na).

Preparation of(R)-1-(2-((1-((6-bromopyridin-2-yl)amino)-3-methyl-1-oxobutan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(6d) Step-1: Preparation of (R)-tert-butyl(1-((6-bromopyridin-2-yl)amino)-3-methyl-1-oxobutan-2-yl)carbamate (6b)

Reaction of (R)-2-((tert-butoxycarbonyl)amino)-3-methylbutanoic acid(6a) (1.0 g, 4.6 mmol) with 6-bromopyridin-2-amine (2b) (1.0 g, 5.80mmol) according to the procedure reported in step-1 of Scheme 2 gaveafter workup and purification by chromatography (R)-tert-butyl(1-((6-bromopyridin-2-yl)amino)-3-methyl-1-oxobutan-2-yl)carbamate (6b)(523 mg, 31% yield) as a white semi-solid; ¹H NMR (300 MHz, DMSO-d₆) δ10.78 (s, 1H), 8.09 (d, J=8.2 Hz, 1H), 7.83-7.66 (m, 1H), 7.34 (d, J=7.6Hz, 1H), 6.97 (d, J=8.4 Hz, 1H), 4.03 (t, J=7.8 Hz, 1H), 2.07-1.87 (m,1H), 1.40 (s, 9H), 0.92-0.84 (m, 6H); MS (ES+): 394.4 (M+Na).

Step-2: Preparation of(R)-2-amino-N-(6-bromopyridin-2-yl)-3-methylbutanamide (6c)

Reaction of (R)-tert-butyl(1-((6-bromopyridin-2-yl)amino)-3-methyl-1-oxobutan-2-yl)carbamate (6b)(490 mg, 1.32 mmol) with TFA (750 mg, 6.58 mmol) according to theprocedure reported in step-2 of Scheme 2 gave after workup andpurification by flash column chromatography [silica (12 g), eluting withMeOH in CHCl₃ 0 to 20%] to give(R)-2-amino-N-(6-bromopyridin-2-yl)-3-methylbutanamide (6c) (185 mg,0.680 mmol, 52% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ8.13 (d, J=8.1 Hz, 1H), 7.74 (t, J=7.9 Hz, 1H), 7.34 (d, J=7.7 Hz, 1H),3.22 (d, J=5.2 Hz, 1H), 2.02-1.85 (m, 1H), 0.91 (d, J=6.8 Hz, 3H), 0.82(d, J=6.8 Hz, 3H); MS (ES+): 272.3 (M+1).

Step-3: Preparation of (R)-tert-butyl(1-((6-bromopyridin-2-yl)amino)-3-methyl-1-oxobutan-2-yl)carbamate (6b)

Reaction of (R)-2-amino-N-(6-bromopyridin-2-yl)-3-methylbutanamide (6c)(91 mg, 0.33 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e)(88 mg, 0.4 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup and purification by chromatography [silica(12 g), eluting with CMA80 in CHCl₃ 0 to 40%] to give (R)-tert-butyl(1-((6-bromopyridin-2-yl)amino)-3-methyl-1-oxobutan-2-yl)carbamate (6b)(65 mg, 0.14 mmol, 41% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 11.12-10.90 (m, 1H), 8.58 (d, J=7.8 Hz, 1H), 8.14 (dd,J=21.5, 8.0 Hz, 2H), 7.84-7.53 (m, 3H), 7.50-7.10 (m, 4H), 5.43-5.19 (m,2H), 4.57-4.34 (m, 1H), 2.18-2.00 (m, 1H), 0.94 (s, 6H); MS (ES+): 473.4(M+1).

Preparation of1-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(7d) Step-1: Preparation of tert-butyl(2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(cyclopropyl) carbamate (7b)

Reaction of 2-((tert-butoxycarbonyl)(cyclopropyl)amino)acetic acid (7a)(0.5 g, 2.32 mmol) with 6-bromopyridin-2-amine (2b) (0.4 g, 2.32 mmol)according to the procedure reported in step-1 of Scheme 2 gave afterworkup and purification by chromatography [silica (12 g), eluting withMeOH in CHCl₃ from 0-20%] tert-butyl(2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(cyclopropyl) carbamate (7b)contaminated with 6-bromopyridin-2-amine (2b).

Step-2: Preparation ofN-(6-bromopyridin-2-yl)-2-(cyclopropylamino)acetamide (7c)

Reaction of tert-butyl(2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(cyclopropyl) carbamate (7b)from above step-1 with TFA (0.9 mL, 11.61 mmol) according to theprocedure reported in step-2 of Scheme 2 gave after workupN-(6-bromopyridin-2-yl)-2-(cyclopropylamino)acetamide (7c) as a TFAsalt; MS (ES+): 272.3 (M+2).

Step-3: Preparation of1-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(7d)

Reaction of N-(6-bromopyridin-2-yl)-2-(cyclopropylamino)acetamide (7c)TFA salt from above step-2 (90 mg, 0.33 mmol) with2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e) (88 mg, 0.4 mmol)according to the procedure reported in step-3 of Scheme 2 gave afterworkup and purification by chromatography [silica (12 g), eluting withCMA80 in CHCl₃ 0 to 40%]1-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(7d) (24 mg, 0.051 mmol, 15% yield for three steps) as a white solid.

¹H NMR (300 MHz, DMSO-d₆) δ 10.96 (s, 1H), 8.17 (d, J=8.1 Hz, 1H), 8.02(d, J=8.1 Hz, 1H), 7.81-7.59 (m, 3H), 7.51-7.18 (m, 4H), 5.70 (s, 2H),4.18 (s, 2H), 3.15-3.05 (m, 1H), 1.15-0.77 (m, 4H); MS (ES+): 471.4(M+1).

Preparation of1-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(methyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(8d) Step-1: Preparation of tert-butyl(2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(methyl)carbamate (8b)

Reaction of 2-((tert-butoxycarbonyl)(methyl)amino)acetic acid (8a) (2 g,10.57 mmol) with 6-bromopyridin-2-amine (2b) (1.52 g, 8.81 mmol)according to the procedure reported in step-1 of Scheme 2 gave afterworkup and purification by chromatography [silica gel (24 g), elutingwith EtOAc (0-50%) in hexane] tert-butyl(2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(methyl)carbamate (8b) (685mg, 1.99 mmol, 23% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ10.90 (d, 1H), 8.06 (t, J=7.8 Hz, 1H), 7.74 (td, J=8.0, 3.6 Hz, 1H),7.34 (d, J=7.7 Hz, 1H), 4.01 (d, J=7.5 Hz, 2H), 2.84 (d, J=8.0 Hz, 3H),1.35 (d, J=27.9 Hz, 9H); MS (ES+): 344.3 (M+1).

Step-2: Preparation of N-(6-bromopyridin-2-yl)-2-(methylamino)acetamide(8c)

Reaction of tert-butyl(2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(methyl)carbamate (8b) (650mg, 1.89 mmol) with TFA (0.73 mL, 9.44 mmol) according to the procedurereported in step-2 of Scheme 2 gave after workup and purification bychromatography [silica (12 g), eluting with MeOH in CHCl₃ 0 to 20%]N-(6-bromopyridin-2-yl)-2-(methylamino)acetamide (8c) (285 mg, 1.17mmol, 62% yield) as an off white solid; ¹H NMR (300 MHz, DMSO-d₆) δ11.38 (s, 1H), 8.93 (s, 2H), 8.05 (d, J=7.9 Hz, 1H), 7.81 (t, J=8.0 Hz,1H), 7.51-7.32 (m, 1H), 3.98 (s, 2H), 2.62 (s, 3H); MS (ES+): 244.3(M+1).

Step-3: Preparation of1-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(methyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(8d)

Reaction of N-(6-bromopyridin-2-yl)-2-(methylamino)acetamide (8c) (90mg, 0.37 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e) (88mg, 0.4 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by chromatography [silica (12 g),eluting with CMA80 in CHCl₃ 0 to 30%]1-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(methyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(8d) (67 mg, 0.15 mmol, 41% yield for three steps) as a yellow solid; ¹HNMR (300 MHz, DMSO-d₆) δ 11.30-10.84 (2 s at 11.22, 10.94, 1H),8.23-8.00 (m, 2H), 7.87-7.56 (m, 3H), 7.49-7.21 (m, 4H), 5.54 (2 s at5.61, 5.46, 2H), 4.34 (2 s at 4.47, 4.20, 2H), 3.04 (2 s at 3.23, 2.85,3H); MS (ES+): 467.4 (M+Na).

Preparation of(S)-1-(2-((1-((3-chloro-2-fluorobenzyl)amino)-1-oxopropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(9e) Step-1: Preparation of (S)-tert-butyl2-(2-(3-carbamoyl-1H-indazol-1-yl)acetamido)propanoate (9b)

Reaction of (5)-tert-butyl 2-aminopropanoate (9a) (767 mg, 4.22 mmol)with 2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e) (1.02 g, 4.64 mmol)according to the procedure reported in step-3 of Scheme 2 gave afterworkup and purification by chromatography [silica (40 g), eluting withCMA80 in CHCl₃ 0 to 40%] (S)-tert-butyl2-(2-(3-carbamoyl-1H-indazol-1-yl)acetamido)propanoate (9b) (965 mg,2.79 mmol, 66% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 8.73(d, J=7.1 Hz, 1H), 8.17 (d, J=8.2 Hz, 1H), 7.77-7.57 (m, 2H), 7.49-7.33(m, 2H), 7.26 (t, J=7.5 Hz, 1H), 5.22 (s, 2H), 4.23-4.06 (m, 1H), 1.38(s, 9H), 1.30 (d, J=7.3 Hz, 3H); MS (ES+): 369.5 (M+Na); 345.4 (M−1).

Step-2: Preparation of(S)-2-(2-(3-carbamoyl-1H-indazol-1-yl)acetamido)propanoic acid (9c)

Reaction of (5)-tert-butyl2-(2-(3-carbamoyl-1H-indazol-1-yl)acetamido)propanoate (9b) (900 mg, 2.6mmol) with TFA (1.2 mL, 15.59 mmol) according to the procedure reportedin step-2 of Scheme 2 gave after workup(S)-2-(2-(3-carbamoyl-1H-indazol-1-yl)acetamido)propanoic acid (9c) (750mg, 2.58 mmol, 99% yield) as a TFA salt which was used in the next stepwithout further purification.

Step-3: Preparation of(S)-1-(2-((1-((3-chloro-2-fluorobenzyl)amino)-1-oxopropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(9e)

Reaction of (S)-2-(2-(3-carbamoyl-1H-indazol-1-yl)acetamido)propanoicacid (9c) (100 mg, 0.35 mmol) TFA salt from above step-2 with3-chloro-2-fluorobenzylamine (9d) (66.0 mg, 0.413 mmol), according tothe procedure reported in step-3 of Scheme 2 gave after workup andpurification by [silica (12 g), eluting with CMA80 in CHCl₃ from 0 to50%](S)-1-(2-((1-((3-chloro-2-fluorobenzyl)amino)-1-oxopropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(9e) (22 mg, 0.05 mmol, 15% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.68 (d, J=7.2 Hz, 1H), 8.64-8.57 (m, 1H), 8.17 (d, J=8.0 Hz,1H), 7.72 (s, 1H), 7.64 (d, J=8.6 Hz, 1H), 7.57-7.33 (m, 3H), 7.34-7.19(m, 2H), 7.19-7.06 (m, 1H), 5.25 (s, 2H), 4.44-4.20 (m, 3H), 1.28 (d,J=6.9 Hz, 3H); MS (ES+): 454.4 (M+Na); 430.4 (M−1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(10c) Step-1: Preparation of tert-butyl(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)carbamate(10a)

Reaction of 2-((tert-butoxycarbonyl)(cyclopropyl)amino)acetic acid (7a)(250 mg, 1.16 mmol) with 3-chloro-2-fluorobenzylamine (9d) (185 mg, 1.16mmol) according to the procedure reported in step-3 of Scheme 2 gaveafter workup and purification by chromatography [silica (40 g), elutingwith EtOAc in hexane 0 to 50%] tert-butyl(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)carbamate(10a) (365 mg, 1.02 mmol, 88% yield) as a clear oil; ¹H NMR (300 MHz,DMSO-d₆) δ 8.42 (t, J=5.9 Hz, 1H), 7.53-7.42 (m, 1H), 7.34-7.23 (m, 1H),7.22-7.11 (m, 1H), 4.33 (d, J=5.7 Hz, 2H), 3.76 (s, 2H), 2.67-2.54 (m,1H), 1.46-1.10 (m, 9H), 0.68-0.43 (m, 4H); MS (ES+): 379.4 (M+Na).

Step-2: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide (10b)

Reaction of tert-butyl(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)carbamate(10a) (365 mg, 1.02 mmol) with TFA (0.54 mL, 6.97 mmol) according to theprocedure reported in step-2 of Scheme 2 gave after workupN-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide (10b) (265 mg,0.715 mmol, 61.5% yield) as a TFA salt, which was used in the next stepwithout further purification; MS (ES+) 257.3 (M+1).

Step-3: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(10c)

Reaction of N-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide(10b) (150 mg, 0.41 mmol) TFA salt from above step-2 with2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e) (106 mg, 0.49 mmol)according to the procedure reported in step-3 of Scheme 2 gave afterworkup and purification by [silica (12 g), eluting with CMA80 in CHCl₃from 0 to 40%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(10c) (85 mg, 0.19 mmol, 46% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.51 (t, J=5.8 Hz, 1H), 8.18 (d, J=8.1 Hz, 1H), 7.74 (s, 1H),7.64 (d, J=8.5 Hz, 1H), 7.52-7.33 (m, 3H), 7.31-7.16 (m, 2H), 7.16-7.05(m, 1H), 5.67 (s, 2H), 4.33 (d, J=5.5 Hz, 2H), 3.98 (s, 2H), 3.14-2.99(m, 1H), 1.08-0.95 (m, 2H), 0.95-0.86 (m, 2H); ¹⁹F NMR (282 MHz, DMSO) δ−121.33; MS (ES+): 458.5 (M+1); 456.5 (M−1).

Preparation of3-(3-(2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)-3-cyclopropylureido)-1H-indole-1-carboxamide(11b)

A suspension of 1-carbamoyl-1H-indole-3-carbonyl azide (11a) (50 mg,0.22 mmol, prepared according to procedure reported by Altmann, Eva etal; in PCT Int. Appl., WO 2012/093101) in toluene (10 mL) was refluxedfor 1.5 h. The resulting clear solution was cooled to room temperatureand added a solution ofN-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide (10b) (56.0mg, 0.22 mmol) in THF (5 mL), and triethylamine (0.061 μL, 0.44 mmol).The reaction mixture was stirred at room temperature for 3 h andconcentrated in vacuum. The residue obtained was purified by flashcolumn chromatography [Silica gel (24 g) eluting with CMA80 in CHCl₃ 0to 40%] to afford3-(3-(2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)-3-cyclopropylureido)-1H-indole-1-carboxamide(11b) (42 mg, 0.092 mmol, 42% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.47 (t, J=5.9 Hz, 1H), 8.33-8.23 (m, 2H), 8.03 (s, 1H), 7.67(d, J=7.7 Hz, 1H), 7.55-7.39 (m, 1H), 7.37-7.23 (m, 2H), 7.23-7.14 (m,2H), 4.36 (d, J=5.7 Hz, 2H), 3.99 (s, 2H), 2.99-2.84 (m, 1H), 1.01-0.88(m, 2H), 0.80 (d, J=3.8 Hz, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.33(t, J=6.9 Hz); MS (ES+) 458.5 (M+1).

Preparation of1-(2-(1-(3-chloro-2-fluorobenzylamino)-2-methyl-1-oxopropan-2-ylamino)-2-oxoethyl)-1H-indazole-3-carboxamide(12d) Step-1: Preparation of tert-butyl2-(2-(3-chloro-2-fluorophenyl)propan-2-ylamino)-2-oxoethylcarbamate(12b)

Reaction of 2-(tert-butoxycarbonylamino)-2-methylpropanoic acid (12a)(650 mg, 3.2 mmol) with 3-chloro-2-fluorobenzylamine (9d) (425 mg, 2.67mmol) according to the procedure reported in step-3 of Scheme 2 gaveafter workup and purification by chromatography [silica (12 g), elutingwith EtOAc in hexane from 0-50%] tert-butyl2-(2-(3-chloro-2-fluorophenyl)propan-2-ylamino)-2-oxoethylcarbamate(12b) (752 mg, 2.18 mmol, 82% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.16 (s, 1H), 7.51-7.28 (m, 2H), 7.18-7.04 (m, 1H), 6.99 (s,1H), 4.29 (d, J=5.5 Hz, 2H), 1.46-1.33 (m, 9H), 1.30 (s, 6H); ¹⁹F NMR(282 MHz, DMSO-d₆) δ −121.85; MS (ES+): 345.4 (M+1), 367.4 (M+Na).

Step-2: Preparation of2-amino-N-(2-(3-chloro-2-fluorophenyl)propan-2-yl)acetamide (12c)

Reaction of tert-butyl2-(2-(3-chloro-2-fluorophenyl)propan-2-ylamino)-2-oxoethylcarbamate(12b) (700 mg, 2.030 mmol) with TFA (0.94 mL, 12.18 mmol) according tothe procedure reported in step-2 of Scheme 2 gave after workup2-amino-N-(2-(3-chloro-2-fluorophenyl)propan-2-yl)acetamide (12c) TFAsalt (725 mg, 2.02 mmol, 100% yield) as a semi-solid, which was used inthe next step without further purification; ¹H NMR (300 MHz, DMSO-d₆)8.93 (t, J=5.6 Hz, 1H), 8.21 (s, 2H), 7.50 (td, J=7.4, 2.1 Hz, 1H),7.31-7.14 (m, 2H), 4.40 (d, J=5.5 Hz, 2H), 1.48 (s, 6H); ¹⁹F NMR (282MHz, DMSO) δ −73.40, −121.12; MS (ES+): 245.3 (M+1).

Step-3: Preparation of1-(2-(1-(3-chloro-2-fluorobenzylamino)-2-methyl-1-oxopropan-2-ylamino)-2-oxoethyl)-1H-indazole-3-carboxamide(12d)

Reaction of 2-amino-N-(2-(3-chloro-2-fluorophenyl)propan-2-yl)acetamide(12c) (300 mg, 0.836 mmol) TFA salt from above step-2 with2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e) (220 mg, 1.0 mmol)according to the procedure reported in step-3 of Scheme 2 gave afterworkup and purification by [silica (12 g), eluting with CMA80 in CHCl₃from 0 to 40%]1-(2-(1-(3-chloro-2-fluorobenzylamino)-2-methyl-1-oxopropan-2-ylamino)-2-oxoethyl)-1H-indazole-3-carboxamide(12d) (185 mg, 0.42 mmol, 50% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.58 (s, 1H), 8.36 (t, J=5.9 Hz, 1H), 8.19 (d, J=8.1 Hz, 1H),7.69 (s, 1H), 7.62-7.53 (m, 1H), 7.46-7.32 (m, 3H), 7.30-7.14 (m, 2H),6.92 (t, J=7.9 Hz, 1H), 5.24 (s, 2H), 4.32 (d, J=5.6 Hz, 2H), 1.41 (s,6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.89; MS (ES+) 446.5 (M+1), 468.5(M+Na).

Preparation of(R)-1-(2-((1-((3-chloro-2-fluorobenzyl)amino)-3-methoxy-1-oxopropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(13d) Step-1: Preparation of (R)-tert-butyl(1-((3-chloro-2-fluorobenzyl)amino)-3-methoxy-1-oxopropan-2-yl)carbamate(13b)

Reaction of (R)-2-((tert-butoxycarbonyl)amino)-3-methoxypropanoic acid(13a) (382 mg, 1.74 mmol) with 3-chloro-2-fluorobenzylamine (9d) (232mg, 1.45 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup (R)-tert-butyl(1-((3-chloro-2-fluorobenzyl)amino)-3-methoxy-1-oxopropan-2-yl)carbamate(13b) which was used as such in next step; MS (ES+): 383.4 (M+Na).

Step-2: Preparation of(R)-2-amino-N-(3-chloro-2-fluorobenzyl)-3-methoxypropanamide (13c)

Reaction of (R)-tert-butyl(1-((3-chloro-2-fluorobenzyl)amino)-3-methoxy-1-oxopropan-2-yl)carbamate(13b) (525 mg, 1.45 mmol) with TFA (2.02 mL, 26.2 mmol) according to theprocedure reported in step-2 of Scheme 2 gave after workup(R)-2-amino-N-(3-chloro-2-fluorobenzyl)-3-methoxypropanamide (13c) TFAsalt (379 mg, 1.45 mmol, 100% yield) which was used in the next stepwithout further purification; MS (ES+): 261.3 (M+1).

Step-3: Preparation of(R)-1-(2-((1-((3-chloro-2-fluorobenzyl)amino)-3-methoxy-1-oxopropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(13d)

Reaction of (R)-2-amino-N-(3-chloro-2-fluorobenzyl)-3-methoxypropanamide(13c) (379 mg, 1.45 mmol) TFA salt from above step-2 with2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e) (382 mg, 1.75 mmol)according to the procedure reported in step-3 of Scheme 2 gave afterworkup and purification by chromatography [silica (24 g), eluting withMeOH in CHCl₃ from 0 to 40%](R)-1-(2-((1-((3-chloro-2-fluorobenzyl)amino)-3-methoxy-1-oxopropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(13d) (32 mg, 5% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ8.78-8.66 (m, 2H), 8.18 (dt, J=8.2, 1.0 Hz, 1H), 7.72 (s, 1H, D₂Oexchangeable), 7.64 (d, J=8.5 Hz, 1H), 7.54-7.35 (m, 3H, 1H, D₂Oexchangeable), 7.31-7.22 (m, 2H), 7.20-7.10 (m, 1H), 5.30 (d, J=2.3 Hz,2H), 4.57-4.47 (m, 1H), 4.46-4.28 (m, 2H), 3.65-3.50 (m, 2H), 3.28 (s,3H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.28; MS (ES+): 484.5 (M+Na); (ES−)496.4 (M+Cl).

Preparation of1-(2-((1-((3-chloro-2-fluorobenzyl)carbamoyl)cyclopentyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(14d) Step-1: Preparation oftert-butyl(1-((3-chloro-2-fluorobenzyl)carbamoyl)cyclopentyl)carbamate(14b)

Reaction of 1-((tert-butoxycarbonyl)amino)cyclopentanecarboxylic acid(14a) (650 mg, 2.85 mmol) with 3-chloro-2-fluorobenzylamine (9d) (379mg, 2.37 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by chromatography [silica gel (12 g),eluting with EtOAc in hexane, 0-50%] tert-butyl(1-((3-chloro-2-fluorobenzyl)carbamoyl)cyclopentyl)carbamate (14b) (650mg, 1.73 mmol, 74% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆)8.15-8.06 (m, 1H), 7.43 (t, J=7.1 Hz, 1H), 7.35 (t, J=7.1 Hz, 1H),7.19-7.06 (m, 2H), 4.31 (d, J=5.9 Hz, 2H), 2.07-1.92 (m, 2H), 1.89-1.71(m, 3H), 1.65-1.55 (m, 3H), 1.38 (s, 9H); MS (ES+): 371.4 (M+1), 393.4(M+Na).

Step-2: Preparation of1-amino-N-(3-chloro-2-fluorobenzyl)cyclopentanecarboxamide (14c)

Reaction of tert-butyl(1-((3-chloro-2-fluorobenzyl)carbamoyl)cyclopentyl)carbamate (14b) (650mg, 1.75 mmol) with TFA (1.35 mL, 17.53 mmol) according to the procedurereported in step-2 of Scheme 2 gave after workup1-amino-N-(3-chloro-2-fluorobenzyl)cyclopentanecarboxamide (14c) TFAsalt (675 mg, 1.75 mmol, 100% yield) as a clear oil which was used inthe next step without further purification; ¹H NMR (300 MHz, DMSO-d₆) δ8.86 (t, J=5.2 Hz, 1H), 8.17 (s, 2H), 7.50 (t, J=7.4 Hz, 1H), 7.32-7.13(m, 2H), 4.40 (d, J=5.2 Hz, 2H), 4.13 (s, 1H), 2.10 (s, 2H), 1.86 (d,J=15.6 Hz, 6H); ¹⁹F NMR (282 MHz, DMSO) δ −73.25 (TFA); −121.06; MS(ES+): 271.3 (M+1).

Step-3: Preparation of1-(2-((1-((3-chloro-2-fluorobenzyl)carbamoyl)cyclopentyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(14d)

Reaction of 1-amino-N-(3-chloro-2-fluorobenzyl)cyclopentanecarboxamide(14c) (117 mg, 0.53 mmol) TFA salt from above step-2 with2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e) (116 mg, 0.53 mmol)according to the procedure reported in step-3 of Scheme 2 gave afterworkup and purification by chromatography [silica (12 g), eluting withCMA80 in CHCl₃ 0 to 40%]1-(2-((1-((3-chloro-2-fluorobenzyl)carbamoyl)cyclopentyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(14d) (62 mg, 0.13 mmol, 30% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.63 (s, 1H), 8.37 (t, J=5.9 Hz, 1H), 8.17 (d, J=8.1 Hz, 1H),7.65 (s, 1H), 7.57 (d, J=8.5 Hz, 1H), 7.45-7.31 (m, 3H), 7.31-7.20 (m,1H), 7.20-7.09 (m, 1H), 6.91 (t, J=7.9 Hz, 1H), 5.25 (s, 2H), 4.33 (d,J=5.7 Hz, 2H), 2.15-1.97 (m, 2H), 1.96-1.80 (m, 2H), 1.77-1.59 (m, 4H);¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.99; MS (ES+): 472.5 (M+1).

Preparation of(S)-1-(2-((1-((3-chloro-2-fluorobenzyl)amino)-1-oxo-3-phenylpropan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(15d) Step-1: Preparation of (S)-tert-butyl(1-((3-chloro-2-fluorobenzyl)amino)-1-oxo-3-phenylpropan-2-yl)carbamate(15b)

Reaction of (S)-2-((tert-butoxycarbonyl)amino)-3-phenylpropanoic acid(15a) (475 mg, 1.79 mmol) with 3-chloro-2-fluorobenzylamine (9d) (238mg, 1.49 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup (5)-tert-butyl(1-((3-chloro-2-fluorobenzyl)amino)-1-oxo-3-phenylpropan-2-yl)carbamate(15b) which was used as such in the next step; MS (ES−): 441.4 (M+Cl).

Step-2: Preparation of(S)-2-amino-N-(3-chloro-2-fluorobenzyl)-3-phenylpropanamide (15c)

Reaction of (5)-tert-butyl(1-((3-chloro-2-fluorobenzyl)amino)-1-oxo-3-phenylpropan-2-yl)carbamate(15b) (607 mg, 1.5 mmol) with TFA according to the procedure reported instep-2 of Scheme 2 gave after workup(S)-2-amino-N-(3-chloro-2-fluorobenzyl)-3-phenylpropanamide (15c) TFAsalt (458 mg, 1.49 mmol, 83%) which was used in next step withoutfurther purification; MS (ES+): 307.4 (M+1), (ES−) 305.2 (M−1).

Step-3: Preparation of(S)-1-(2-((1-((3-chloro-2-fluorobenzyl)amino)-1-oxo-3-phenylpropan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(15d)

Reaction of (S)-2-amino-N-(3-chloro-2-fluorobenzyl)-3-phenylpropanamide(15c) (458 mg, 1.49 mmol) TFA salt from above step-2 with2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e) (393 mg, 1.79 mmol)according to the procedure reported in step-3 of Scheme 2 gave afterworkup and purification by chromatography [silica (24 g), eluting withMeOH in CHCl₃ 0 to 40%](S)-1-(2-((1-((3-chloro-2-fluorobenzyl)amino)-1-oxo-3-phenylpropan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(15d) (66 mg, 13% yield) as an off-white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.79-8.67 (m, 2H), 8.15 (dt, J=8.2, 1.0 Hz, 1H), 7.65 (s,1H), 7.47 (td, J=7.5, 1.9 Hz, 1H), 7.42-7.35 (m, 3H), 7.30-7.19 (m, 6H),7.14-7.00 (m, 2H), 5.31-5.08 (m, 2H), 4.64-4.53 (m, 1H), 4.44-4.21 (m,2H), 3.11-2.97 (m, 1H), 2.92-2.75 (m, 1H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.21; MS (ES+): 530.5 (M+Na); (ES−): 506.5 (M−1), 542.4 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(16d) Step-1: Preparation of tert-butyl(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)carbamate (16b)

Reaction of 2-((tert-butoxycarbonyl)amino)acetic acid (16a) (4 g, 22.83mmol) with 3-chloro-2-fluorobenzylamine (9d) (3.31 g, 20.76 mmol)according to the procedure reported in step-3 of Scheme 2 gave afterworkup and purification by chromatography [silica (80 g), eluting withEtOAc in hexane from 0 to 60%] tert-butyl(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)carbamate (16b) (4.09 g,12.91 mmol, 62% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ8.37 (t, J=5.8 Hz, 1H), 7.53-7.41 (m, 1H), 7.35-7.23 (m, 1H), 7.24-7.12(m, 1H), 7.05 (t, J=6.0 Hz, 1H), 4.33 (d, J=5.8 Hz, 2H), 3.57 (d, 2H),1.38 (s, 9H); ¹⁹F NMR (282 MHz, DMSO) δ −121.38; MS (ES+): 339.4 (M+Na)

Step-2: Preparation of 2-amino-N-(3-chloro-2-fluorobenzyl)acetamide(16c)

Reaction of tert-butyl(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)carbamate (16b) (4.08 g,12.88 mmol) with TFA (4.96 mL, 64.4 mmol) according to the procedurereported in step-2 of Scheme 2 gave after workup2-amino-N-(3-chloro-2-fluorobenzyl)acetamide (16c) TFA salt (9.07 mmol,70% yield) as a white solid, which was used in the next step withoutfurther purification; ¹H NMR (300 MHz, DMSO-d₆) δ 8.94 (t, J=5.7 Hz,1H), 8.04 (s, 3H), 7.56-7.45 (m, 1H), 7.40-7.29 (m, 1H), 7.27-7.15 (m,1H), 4.41 (d, J=5.7 Hz, 2H), 3.62 (s, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−73.32, −120.87; MS (ES⁺) 217.2 (M+1).

Step-3: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(16d) Reaction of 2-amino-N-(3-chloro-2-fluorobenzyl)acetamide (16c)

(160 mg, 0.48 mmol) TFA salt from above step-2 with2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e) (127 mg, 0.58 mmol)according to the procedure reported in step-3 of Scheme 2 gave afterworkup and purification by chromatography [silica (12 g), eluting withCMA80 in CHCl₃ 0 to 40%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(16d) (120 mg, 0.29 mmol, 59% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.59 (t, J=5.7 Hz, 1H), 8.54 (t, J=5.7 Hz, 1H), 8.18 (d,J=8.0 Hz, 1H), 7.75-7.61 (m, 2H), 7.54-7.34 (m, 3H), 7.33-7.20 (m, 2H),7.20-7.10 (m, 1H), 5.26 (s, 2H), 4.36 (d, J=5.6 Hz, 2H), 3.82 (d, J=5.5Hz, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.23; MS (ES+): 418.5 (M+1),440.4 (M+Na); 416.3 (M−1).

Preparation of3-(3-(2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)-3-cyclopropylureido)-1H-indole-1-carboxamide(17a)

Reaction of N-(6-bromopyridin-2-yl)-2-(cyclopropylamino)acetamide (7c)with 1-carbamoyl-1H-indole-3-carbonyl azide (11a) (50 mg, 0.22 mmol)according to the procedure reported in Scheme 11 gave after workup andpurification by flash column chromatography (Silica gel, 24 g elutingwith CHCl₃-CMA80 0-40%)3-(3-(2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)-3-cyclopropylureido)-1H-indole-1-carboxamide(17a) (108 mg, 0.23 mmol, 76% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 10.95 (s, 1H), 8.35-8.22 (m, 2H), 8.07 (d, J=8.2 Hz, 1H),8.02 (s, 1H), 7.78-7.64 (m, 2H), 7.42 (s, 2H), 7.34 (d, J=7.7 Hz, 1H),7.31-7.15 (m, 2H), 4.19 (s, 2H), 3.06-2.89 (m, 1H), 1.05-0.87 (m, 2H),0.85-0.72 (m, 2H); MS (ES+): 471.4 (M+1), 493.4 (M+Na).

Preparation of(S)-1-(2-((1-((3-chloro-2-fluorobenzyl)amino)-1-oxohexan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(18d) Step-1: Preparation of (5)-tert-butyl(1-((3-chloro-2-fluorobenzyl)amino)-1-oxohexan-2-yl)carbamate (18b)

Reaction of (S)-2-((tert-butoxycarbonyl)amino)hexanoic acid (18a) (0.42g, 1.8 mmol) with 3-chloro-2-fluorobenzylamine (9d) (0.239 g, 1.5 mmol)according to the procedure reported in step-3 of Scheme 2 gave afterworkup (5)-tert-butyl(1-((3-chloro-2-fluorobenzyl)amino)-1-oxohexan-2-yl)carbamate (18b)which was used as such in the next step.

Step-2: Preparation of (S)-2-amino-N-(3-chloro-2-fluorobenzyl)hexanamide(18c)

Reaction of (5)-tert-butyl(1-((3-chloro-2-fluorobenzyl)amino)-1-oxohexan-2-yl)carbamate (18b)(0.56 g, 1.5 mmol) with TFA (2.08 mL, 26.9 mmol) according to theprocedure reported in step-2 of Scheme 2 gave after workup(S)-2-amino-N-(3-chloro-2-fluorobenzyl)hexanamide (18c) TFA salt (9.07mmol, 70% yield) which was used as such in the next step; MS (ES+):273.4 (M+1).

Step-3: Preparation of(S)-1-(2-((1-((3-chloro-2-fluorobenzyl)amino)-1-oxohexan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(18d)

Reaction of (S)-2-amino-N-(3-chloro-2-fluorobenzyl)hexanamide (18c) (408mg, 1.5 mmol) TFA salt from above step-2 with2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e) (393 mg, 1.8 mmol)according to the procedure reported in step-3 of Scheme 2 gave afterworkup gave(S)-1-(2-((1-((3-chloro-2-fluorobenzyl)amino)-1-oxohexan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(18d) (56 mg, 0.12 mmol, 8% yield) as an off-white solid; ¹H NMR (300MHz, DMSO-d₆) δ 8.76-8.62 (m, 2H, D₂O exchangeable), 8.24 (d, J=8.1 Hz,1H), 7.76 (s, 1H, D₂O exchangeable), 7.69 (d, J=8.6 Hz, 1H), 7.60-7.42(m, 3H), 7.32 (t, J=7.7 Hz, 2H), 7.20 (t, J=7.8 Hz, 1H), 5.32 (s, 2H),4.53-4.26 (m, 3H), 1.81-1.56 (m, 2H), 1.31 (s, 4H), 0.96-0.86 (m, 3H);¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.09; MS (ES+): 496.5 (M+Na), 472.5(M−1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(19d) Step-1: Preparation of tert-butyl(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)carbamate(19b)

Reaction of 2-((tert-butoxycarbonyl)(isopropyl)amino)acetic acid (19a)(300 mg, 1.38 mmol) with 3-chloro-2-fluorobenzylamine (9d) (200 mg, 1.26mmol) according to the procedure reported in step-3 of Scheme 2 gaveafter workup and purification by chromatography [silica (12 g), elutingwith EtOAc in hexane 0 to 60%] tert-butyl(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)carbamate(19b) (395 mg, 1.1 mmol, 88% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.35 (s, 1H), 7.47 (t, J=7.5 Hz, 1H), 7.37-7.25 (m, 1H),7.23-7.10 (m, 1H), 4.32 (d, J=5.7 Hz, 2H), 4.28-3.95 (m, 1H), 3.75-3.57(m, 2H), 1.40 (s, 3H), 1.26 (s, 6H), 1.12-0.95 (m, 6H); MS (ES⁺) 381.4(M+Na).

Step-2: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide (19c)

Reaction of tert-butyl(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)carbamate(19b) (340 mg, 0.95 mmol) with TFA (0.37 mL, 4.74 mmol) according to theprocedure reported in step-2 of Scheme 2 gave after workupN-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide (19c) TFA salt(348 mg, 0.93 mmol, 99% yield) as a white solid, which was used in thenext step without further purification; ¹H NMR (300 MHz, DMSO-d₆) δ 9.04(t, J=5.7 Hz, 1H), 8.81 (s, 2H), 7.57-7.46 (m, 1H), 7.40-7.30 (m, 1H),7.26-7.16 (m, 1H), 4.42 (d, J=5.6 Hz, 2H), 3.78-3.77 (m, 2H), 3.37-3.20(m, 1H), 1.20 (d, J=6.5 Hz, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −73.83(TFA peak), −120.79; MS (ES+) 259.4 (M+1).

Step-3: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(19d)

Reaction of N-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide(19c) (160 mg, 0.43 mmol) TFA salt from above step-2 with2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e) (113 mg, 0.52 mmol)according to the procedure reported in step-3 of Scheme 2 gave afterworkup and purification by chromatography [silica (12 g), eluting withCMA80 in CHCl₃ 0 to 40%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(19d) (115 mg, 0.25 mmol, 58% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.83, 8.36 (2t, J=5.7 Hz, 1H), 8.18 (d, J=8.0 Hz, 1H), 7.71(s, 1H), 7.63-7.47 (m, 2H), 7.47-7.31 (m, 3H), 7.29-6.99 (m, 2H), 5.59,5.45 (2s, 2H), 4.61-4.39 (m, 2H), 4.36-4.10 (m, 2H), 3.91-3.75 (m, 1H),1.23, 0.99 (2dd, J=72.0, 6.4 Hz, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−120.94, −121.48; MS (ES+): 460.5 (M+1); (ES−): 458.5 (M−1); (based onNMR the compound is a mixture of rotamers with 2:3 ratio)

Preparation of(S)-1-(2-((1-((3-chloro-2-fluorobenzyl)amino)-1-oxo-3-(thiophen-2-yl)propan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(20d) Step-1: Preparation of (5)-tert-butyl(1-((3-chloro-2-fluorobenzyl)amino)-1-oxo-3-(thiophen-2-yl)propan-2-yl)carbamate(20b)

Reaction of(S)-2-((tert-butoxycarbonyl)amino)-3-(thiophen-2-yl)propanoic acid (20a)(428 mg, 1.58 mmol) with 3-chloro-2-fluorobenzylamine (9d) (252 mg, 1.58mmol) according to the procedure reported in step-3 of Scheme 2 gaveafter workup (5)-tert-butyl(1-((3-chloro-2-fluorobenzyl)amino)-1-oxo-3-(thiophen-2-yl)propan-2-yl)carbamate(20b) which was used as such in the next step; MS (ES−): 448.4 (M+Cl).

Step-2: Preparation of(S)-2-amino-N-(3-chloro-2-fluorobenzyl)-3-(thiophen-2-yl)propanamide(20c)

Reaction of(S)-tert-butyl(1-((3-chloro-2-fluorobenzyl)amino)-1-oxo-3-(thiophen-2-yl)propan-2-yl)carbamate(20b) (652 mg, 1.58 mmol) with TFA (2.19 mL, 28.4 mmol) according to theprocedure reported in step-2 of Scheme 2 gave after workup(S)-2-amino-N-(3-chloro-2-fluorobenzyl)-3-(thiophen-2-yl)propanamide(20c) TFA salt which was used in next step without further purification;MS (ES+): 313.3 (M+1).

Step-3: Preparation of(S)-1-(2-((1-((3-chloro-2-fluorobenzyl)amino)-1-oxo-3-(thiophen-2-yl)propan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(20d)

Reaction of (S)-2-amino-N-(3-chloro-2-fluorobenzyl)-3-phenylpropanamide(15c) (494 mg, 1.58 mmol) TFA salt from above step-2 with2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e) (415 mg, 1.9 mmol)according to the procedure reported in step-3 of Scheme 2 gave afterworkup(S)-1-(2-((1-((3-chloro-2-fluorobenzyl)amino)-1-oxo-3-(thiophen-2-yl)propan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(20d) (86 mg, 11% yield) as an off-white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.91-8.70 (m, 2H), 8.17 (dt, J=8.2, 1.0 Hz, 1H), 7.67 (s,1H), 7.55-7.35 (m, 5H), 7.30-7.21 (m, 1H), 7.17-7.04 (m, 2H), 6.98-6.92(m, 1H), 6.92-6.87 (m, 1H), 5.37-5.09 (m, 2H), 4.66-4.50 (m, 1H),4.46-4.22 (m, 2H), 3.33-3.21 (m, 1H), 3.17-2.99 (m, 1H); ¹⁹F NMR (282MHz, DMSO-d₆) δ −121.19; MS (ES+): 514.53 (M+1), 536.5 (M+Na), 512.5(M−1).

Preparation of(S)-1-(2-((1-((3-chloro-2-fluorobenzyl)amino)-4-(methylthio)-1-oxobutan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(21d) Step-1: Preparation of (5)-tert-butyl(1-((3-chloro-2-fluorobenzyl)amino)-4-(methylthio)-1-oxobutan-2-yl)carbamate(21b)

Reaction of (S)-2-((tert-butoxycarbonyl)amino)-4-(methylthio)butanoicacid (21a) (391 mg, 1.57 mmol) with 3-chloro-2-fluorobenzylamine (9d)(250 mg, 1.57 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup (5)-tert-butyl(1-((3-chloro-2-fluorobenzyl)amino)-4-(methylthio)-1-oxobutan-2-yl)carbamate(21b) which was used as such in the next step; MS (ES−): 391.4 (M−1).

Step-2: Preparation of(S)-2-amino-N-(3-chloro-2-fluorobenzyl)-4-(methylthio)butanamide (21c)

Reaction of (5)-tert-butyl(1-((3-chloro-2-fluorobenzyl)amino)-4-(methylthio)-1-oxobutan-2-yl)carbamate(21b) from above step with TFA (3 mL) according to the procedurereported in step-2 of Scheme 2 gave after workup(S)-2-amino-N-(3-chloro-2-fluorobenzyl)-4-(methylthio)butanamide (21c)TFA salt which was used in next step without further purification; MS(ES+): 291.3 (M+1).

Step-3: Preparation of(S)-1-(2-((1-((3-chloro-2-fluorobenzyl)amino)-4-(methylthio)-1-oxobutan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(21d)

Reaction of(S)-2-amino-N-(3-chloro-2-fluorobenzyl)-4-(methylthio)butanamide (21c)(0.254 g, 0.931 mmol) TFA salt from above step-2 with2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e) (136 mg, 0.62 mmol)according to the procedure reported in step-3 of Scheme 2 gave afterworkup and purification by flash column chromatography [silica gel (24g), eluting with CMA80 in CHCl₃ 0 to 40%](5)-1-(2-((1-((3-chloro-2-fluorobenzyl)amino)-4-(methylthio)-1-oxobutan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(21d) (33 mg, 0.067 mmol, 11% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.75-8.60 (m, 2H), 8.17 (d, J=8.1 Hz, 1H), 7.71 (s, 1H), 7.63(d, J=8.5 Hz, 1H), 7.58-7.35 (m, 3H), 7.31-7.20 (m, 2H), 7.15 (q, J=8.8,7.8 Hz, 1H), 5.27 (s, 2H), 4.47-4.27 (m, 3H), 2.48-2.36 (m, 2H), 2.04(s, 1H), 2.02 (s, 2H), 2.01-1.67 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.12 (d, J=7.1 Hz); MS (ES+): 492.5 (M+1); MS (ES−): 490.5 (M−1);526.5 (M+Cl).

Preparation of(S)-1-(2-((1-((3-chloro-2-fluorobenzyl)amino)-4-methyl-1-oxopentan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(22d) Step-1: Preparation of (S)-tert-butyl(1-((3-chloro-2-fluorobenzyl)amino)-4-methyl-1-oxopentan-2-yl)carbamate(22b)

Reaction of (S)-2-((tert-butoxycarbonyl)amino)-4-methylpentanoic acid(22a) (362 mg, 1.57 mmol) with 3-chloro-2-fluorobenzylamine (9d) (250mg, 1.57 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup (5)-tert-butyl(1-((3-chloro-2-fluorobenzyl)amino)-4-methyl-1-oxopentan-2-yl)carbamate(22b) which was used as such in the next step; MS (ES+): 395.4 (M+Na).

Step-2: Preparation of(S)-2-amino-N-(3-chloro-2-fluorobenzyl)-4-methylpentanamide (22c)

Reaction of (5)-tert-butyl(1-((3-chloro-2-fluorobenzyl)amino)-4-methyl-1-oxopentan-2-yl)carbamate(22b) from above step with TFA (3 mL) according to the procedurereported in step-2 of Scheme 2 gave after workup(S)-2-amino-N-(3-chloro-2-fluorobenzyl)-4-methylpentanamide (22c) TFAsalt which was used in next step without further purification; MS (ES+):273.4 (M+1).

Step-3: Preparation of(S)-1-(2-((1-chloro-2-fluorobenzyl)amino)-4-methyl-1-oxopentan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(22d)

Reaction of (S)-2-amino-N-(3-chloro-2-fluorobenzyl)-4-methylpentanamide(22c) (0.25 g, 0.93 mmol) TFA salt from above step-2 with2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e) (136 mg, 0.62 mmol)according to the procedure reported in step-3 of Scheme 2 gave afterworkup and purification by flash column chromatography [silica gel (24g), eluting with CMA80 in CHCl₃; 0 to 40%](S)-1-(2-((1-((3-chloro-2-fluorobenzyl)amino)-4-methyl-1-oxopentan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(22d) (65 mg, 0.14 mmol, 22% yield) as a pale white solid; ¹H NMR (300MHz, DMSO-d₆) δ 8.69 (t, J=5.8 Hz, 1H), 8.62 (d, J=8.0 Hz, 1H), 8.17 (d,J=8.1 Hz, 1H), 7.70 (s, 1H), 7.61 (d, J=8.5 Hz, 1H), 7.52-7.35 (m, 3H),7.32-7.19 (m, 2H), 7.13 (t, J=7.9 Hz, 1H), 5.25 (s, 2H), 4.42-4.24 (m,3H), 1.70-1.54 (m, 1H), 1.55-1.42 (m, 2H), 0.90 (d, J=6.4 Hz, 3H), 0.83(d, J=6.4 Hz, 3H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.23; MS (ES+) 474.5(M+1), 496.5 (M+Na); MS (ES−) 508.5

Preparation of(S)-1-(2-((1-((3-chlorobenzyl)amino)-1-oxopropan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(23b)

Reaction of (S)-2-(2-(3-carbamoyl-1H-indazol-1-yl)acetamido)propanoicacid (9c) (200 mg, 0.69 mmol) TFA salt with (3-chlorophenyl)methanamine(23a) (98 mg, 0.69 mmol), according to the procedure reported in step-3of Scheme 2 gave after workup(S)-1-(2-((1-((3-chlorobenzyl)amino)-1-oxopropan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(23b) (126 mg, 0.3 mmol, 44% yield) as a yellow solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.67 (d, J=7.4 Hz, 1H), 8.59 (t, J=6.0 Hz, 1H), 8.17 (d,J=8.1 Hz, 1H), 7.72 (s, 1H), 7.64 (d, J=8.5 Hz, 1H), 7.47-7.15 (m, 7H),5.41-5.16 (m, 2H), 4.43-4.23 (m, 3H), 1.29 (d, J=7.0 Hz, 3H); MS (ES+):414.5 (M+1); ES(−): 412.4 (M−1).

Preparation of1-(2-(benzyl(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(24b) Step-1: Preparation of2-(benzylamino)-N-(3-chloro-2-fluorobenzyl)acetamide (24a)

To a solution of 2-amino-N-(3-chloro-2-fluorobenzyl)acetamide (16c) (320mg, 1.48 mmol) in THF (10 mL) was added benzaldehyde (143 mg, 1.343mmol) and acetic acid (0.12 mL, 2.01 mmol). The resulting mixture wasstirred for 50 min, NaBH₄ (102 mg, 2.69 mmol) was added and stirred atroom temperature overnight. The reaction was quenched with aqueousNaHCO₃ (2N, 20 mL), stirred for 30 min- and diluted with EtOAc (100 mL).The organic layer was separated washed with brine, dried, filtered andconcentrated in vacuum to afford2-(benzylamino)-N-(3-chloro-2-fluorobenzyl)acetamide (24a) (240 mg, 0.78mmol, 58% yield). which was used in the next step without furtherpurification. MS (ES+): 307.3 (M+1)

Step-2: Preparation of1-(2-(benzyl(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(24b)

Reaction of 2-(benzylamino)-N-(3-chloro-2-fluorobenzyl)acetamide (24a)(240 mg, 0.78 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e)(171 mg, 0.78 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup and purification by chromatography [silica(12 g), eluting with CMA80 in CHCl₃; 0 to 40%]1-(2-(benzyl(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(24b) (38 mg, 0.075 mmol, 10% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.79 and 8.52 (2t, J=5.9 Hz, 1H), 8.25-8.11 (m, 1H),7.80-7.66 (m, 1H), 7.66-7.56 (m, 1H), 7.56-7.36 (m, 5H), 7.34-7.10 (m,6H), 5.58 (s, 2H), 4.83 and 4.46 (2s, 2H), 4.43 and 4.34 (2d, J=5.6 Hz,2H), 4.21 and 3.95 (s, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.06,−121.35; MS (ES+): 508.5 (M+1); (ES−) 506.5 (M−1); (based on NMR thecompound is a mixture of rotamers 2:1 ratio)

Preparation of3-(3-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-3-isopropylureido)-1H-indole-1-carboxamide(25a)

Reaction of N-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide(19c) (90 mg, 0.35 mmol) with 1-carbamoyl-1H-indole-3-carbonyl azide(11a) (80 mg, 0.35 mmol) according to the procedure reported in Scheme11 gave after workup and purification by flash column chromatography(Silica gel, 24 g eluting with CMA80 in CHCl₃ from 0-30%)3-(3-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-3-isopropylureido)-1H-indole-1-carboxamide(25a) (9 mg, 6% yield) as a yellow solid; ¹H NMR (300 MHz, DMSO-d₆) δ8.92 (s, 1H, D20 exchangeable), 8.82-8.70 (m, 1H, D₂O exchangeable),8.30-8.22 (m, 1H), 7.98 (s, 1H), 7.62 (d, J=7.7 Hz, 1H), 7.54-7.32 (m,4H, 2H, D₂O exchangeable), 7.30-7.21 (m, 1H), 7.20-7.11 (m, 2H),4.56-4.33 (m, 3H), 3.97 (s, 2H), 1.10 (d, J=6.6 Hz, 6H); ¹⁹F NMR (282MHz, DMSO-d₆) δ −121.07; MS (ES+): 460.5 (M+1), 482.49 (M+Na); MS (ES−):458.44 (M−1).

Preparation of(S)-1-(2-((1-((3-chloro-2-fluorobenzyl)amino)-3-hydroxy-1-oxopropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(26d) Step-1: Preparation of (S)-tert-butyl(1-((3-chloro-2-fluorobenzyl)amino)-3-hydroxy-1-oxopropan-2-yl)carbamate(26b)

Reaction of (S)-2-((tert-butoxycarbonyl)amino)-3-hydroxypropanoic acid(26a) (389 mg, 1.9 mmol) with 3-chloro-2-fluorobenzylamine (9d) (252 mg,1.58 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup (5)-tert-butyl(1-((3-chloro-2-fluorobenzyl)amino)-3-hydroxy-1-oxopropan-2-yl)carbamate(26b) which was used as such in the next step; MS (ES+): 369.4 (M+Na),MS (ES−): 381.3 (M+Cl).

Step-2: Preparation of(S)-2-amino-N-(3-chloro-2-fluorobenzyl)-3-hydroxypropanamide (26c)

Reaction of (5)-tert-butyl(1-((3-chloro-2-fluorobenzyl)amino)-3-hydroxy-1-oxopropan-2-yl)carbamate(26b) (548 mg, 1.58 mmol) from above step with TFA (2.19 mL, 28.4 mmol)according to the procedure reported in step-2 of Scheme 2 gave afterworkup (S)-2-amino-N-(3-chloro-2-fluorobenzyl)-3-hydroxypropanamide(26c) TFA salt which was used in next step without further purification;MS (ES+): 247.3 (M+1).

Step-3: Preparation of(S)-1-(2-((1-((3-chloro-2-fluorobenzyl)amino)-3-hydroxy-1-oxopropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(26d)

Reaction of (S)-2-amino-N-(3-chloro-2-fluorobenzyl)-3-hydroxypropanamide(26c) (390 g, 1.58 mmol) TFA salt from above step-2 with2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e) (416 mg, 1.9 mmol)according to the procedure reported in step-3 of Scheme 2 gave afterworkup and purification by flash column chromatography [silica gel (24g), eluting with CMA80 in CHCl₃; 0 to 100%](S)-1-(2-((1-((3-chloro-2-fluorobenzyl)amino)-3-hydroxy-1-oxopropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(26d) (16 mg, 2% yield) as an off white solid; ¹H NMR (300 MHz, DMSO-d₆)δ 8.67-8.57 (m, 2H, D₂O exchangeable), 8.18 (dt, J=8.2, 1.0 Hz, 1H),7.73 (s, 1H, D₂O exchangeable), 7.64 (dt, J=8.6, 0.9 Hz, 1H), 7.52-7.37(m, 3H), 7.33-7.22 (m, 2H), 7.17-7.09 (m, 1H), 5.40-5.22 (m, 2H), 5.13(t, J=5.3 Hz, 1H, D₂O exchangeable), 4.42-4.29 (m, 3H), 3.70-3.59 (m,2H); ¹H NMR (300 MHz, DMSO-d₆ D₂O) δ 8.17-8.09 (m, 1H), 7.62-7.55 (m,1H), 7.46-7.36 (m, 2H), 7.34-7.17 (m, 2H), 7.06 (t, J=7.9 Hz, 1H),5.40-5.14 (m, 2H), 4.32 (s, 2H), 4.28 (t, J=5.4 Hz, 1H), 3.76-3.54 (m,2H); MS (ES+): 448.5 (M+1), 470.5 (M+Na); MS (ES−): 446.4 (M−1), 482.4(M+Cl).

Preparation of(S)-1-(2-((1-((3-chloro-2-fluorobenzyl)amino)-3-cyclopropyl-1-oxopropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(27d) Step-1: Preparation of (S)-tert-butyl(1-((3-chloro-2-fluorobenzyl)amino)-3-cyclopropyl-1-oxopropan-2-yl)carbamate(27b)

Reaction of (S)-2-((tert-butoxycarbonyl)amino)-3-cyclopropylpropanoicacid (27a) (575 mg, 2.51 mmol, prepared according to method reported byHendricks, Robert Than et al; in U.S. Pat. Appl. Publ., 20110230462)according to the procedure reported in step-3 of Scheme 2 gave afterworkup(S)-tert-butyl(1-((3-chloro-2-fluorobenzyl)amino)-3-cyclopropyl-1-oxopropan-2-yl)carbamate(27b) which was used as such in the next step; MS (ES+): 393.3 (M+Na);MS (ES−): 405.4 (M+Cl).

Step-2: Preparation of(S)-2-amino-N-(3-chloro-2-fluorobenzyl)-3-cyclopropylpropanamide (27c)

Reaction of (5)-tert-butyl(1-((3-chloro-2-fluorobenzyl)amino)-3-cyclopropyl-1-oxopropan-2-yl)carbamate(27b) (930 mg, 2.51 mmol) from above step with TFA (3.48 mL, 45.1 mmol)according to the procedure reported in step-2 of Scheme 2 gave afterworkup (S)-2-amino-N-(3-chloro-2-fluorobenzyl)-3-cyclopropylpropanamide(27c) TFA salt which was used in next step without further purification;MS (ES+): 271.3 (M+1).

Step-3: Preparation of(S)-1-(2-((1-((3-chloro-2-fluorobenzyl)amino)-3-cyclopropyl-1-oxopropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(27d)

Reaction of(S)-2-amino-N-(3-chloro-2-fluorobenzyl)-3-cyclopropylpropanamide (27c)(679 g, 2.51 mmol) TFA salt from above step-2 with2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e) (660 mg, 3.01 mmol)according to the procedure reported in step-3 of Scheme 2 gave afterworkup(5)-1-(2-((1-((3-chloro-2-fluorobenzyl)amino)-3-cyclopropyl-1-oxopropan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(27d) (93 mg, 8% yield) as an off-white solid; ¹H NMR (300 MHz, DMSO-d₆)δ 8.73-8.56 (m, 2H), 8.17 (d, J=8.1 Hz, 1H), 7.69 (s, 1H), 7.63 (d,J=8.4 Hz, 1H), 7.52-7.36 (m, 3H), 7.25 (t, J=7.4 Hz, 2H), 7.13 (t, J=7.9Hz, 1H), 5.26 (s, 2H), 4.45-4.25 (m, 3H), 1.73-1.36 (m, 2H), 0.79-0.63(m, 1H), 0.46-0.25 (m, 2H), 0.15-0.01 (m, 2H); ¹⁹F NMR (282 MHz,DMSO-d₆) δ 120.97; MS (ES+): 472.5 (M+1), 494.5 (M+Na); (ES−): 470.4(M−1), 506.5 (M+Cl).

Preparation of1-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(28c) Step-1: Preparation of tert-butyl(2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(isopropyl)carbamate (28a)

Reaction of 2-((tert-butoxycarbonyl)(isopropyl)amino)acetic acid (19a)(0.65 g, 2.99 mmol) with 6-bromopyridin-2-amine (2b) (0.78 g, 4.49 mmol)according to the procedure reported in step-1 of Scheme 2 gave afterworkup and purification by chromatography [silica (12 g), eluting withMeOH in CHCl₃ from 0-20%] tert-butyl(2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(isopropyl)carbamate (28a)which was used in the next step without further purification.

Step-2: Preparation ofN-(6-bromopyridin-2-yl)-2-(isopropylamino)acetamide (28b)

Reaction of tert-butyl(2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(isopropyl)carbamate (28a)from above step-1 with TFA (1.15 mL, 14.96 mmol) according to theprocedure reported in step-2 of Scheme 2 gave after workup andpurification by chromatography [silica (12 g), eluting with CMA80 inCHCl₃ 0 to 20%] N-(6-bromopyridin-2-yl)-2-(isopropylamino)acetamide(28b) (340 mg, 1.25 mmol, 42%) which was used in the next step withoutfurther purification; MS (ES+): 272.3 (M+1).

Step-3: Preparation of1-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(28c)

Reaction of N-(6-bromopyridin-2-yl)-2-(isopropylamino)acetamide (28b)(100 mg, 0.26 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e)(62 mg, 0.29 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup and purification by chromatography [silica(12 g), eluting with CMA80 in CHCl₃ 0 to 40%]1-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(28c) (70 mg, 0.15 mmol, 57% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 11.17 and 10.77 (2s, 1H), 8.24-7.95 (m, 2H), 7.87-7.54 (m,3H), 7.51-7.14 (m, 4H), 5.62 and 5.46 (2s, 2H), 4.606-4.332 (m, 1H),4.43 and 4.03 (2s, 2H), 1.25 (d, J=6.3 Hz, 3H), 1.04 (d, J=6.8 Hz, 3H);MS (ES+): 473.4 (M+1); (based on NMR the compound is a mixture ofrotamers with 1.2:1 ratio)

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopentyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(29b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-(isopentylamino)acetamide (29a)

Reaction of 2-amino-N-(3-chloro-2-fluorobenzyl)acetamide (16c) (337 mg,1.56 mmol) with isovaleraldehyde (147 mg, 1.711 mmol) according to theprocedure reported in step-1 of Scheme 24 gave after work andpurification by flash column chromatography [silica (12 g), eluting withEtOAc in hexane 0 to 60%]N-(3-chloro-2-fluorobenzyl)-2-(isopentylamino)acetamide (29a) (120 mg,0.42 mmol, 27% yield) as a clear oil; ¹H NMR (300 MHz, DMSO-d₆) δ 8.34(t, J=5.8 Hz, 1H), 7.52-7.39 (m, 1H), 7.32-7.23 (m, 1H), 7.21-7.11 (m,1H), 4.36 (d, J=5.9 Hz, 2H), 3.11 (s, 2H), 2.48-2.39 (m, 2H), 1.66-1.43(m, 1H), 1.36-1.16 (m, 3H), 0.82 (d, J=6.6 Hz, 6H); ¹⁹F NMR (282 MHz,DMSO-d₆) δ −121.38; MS (ES+): 287.4 (M+1); (ES−): 285.3 (M−1).

Step-2: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-(isopentylamino)acetamide (29a)

Reaction of N-(3-chloro-2-fluorobenzyl)-2-(isopentylamino)acetamide(29a) (100 mg, 0.35 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (84 mg, 0.384 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by chromatography[silica (12 g), eluting with CMA80 in CHCl₃ 0 to 40%]N-(3-chloro-2-fluorobenzyl)-2-(isopentylamino)acetamide (29a) (100 mg,0.21 mmol, 59% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 8.85and 8.49 (2t, J=5.6 Hz, 1H), 8.18 (d, J=8.1 Hz, 1H), 7.76-7.66 (m, 1H),7.62-7.47 (m, 2H), 7.47-7.33 (m, 3H), 7.29-7.09 (m, 2H), 5.56 and 5.47(2s, 2H), 4.46 and 4.34 (2d, J=5.4 Hz, 2H), 4.23 and 3.94 (2s, 2H),3.52-3.39 (m, 1H), 3.30-3.15 (m, 1H), 1.66-1.37 (m, 2H), 1.37-1.15 (m,1H), 0.93 and 0.80 (2d, J=6.4 Hz, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−120.92, −121.31; MS (ES+): 473.4 (M+1); (based on NMR the compound is amixture of rotamers with 3:2 ratio).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(neopentyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(30b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-(neopentylamino)acetamide (30a)

Reaction of 2-amino-N-(3-chloro-2-fluorobenzyl)acetamide (16c) (300 mg,1.39 mmol) with trimethylacetaldehyde (131 mg, 1.523 mmol) according tothe procedure reported in step-1 of Scheme 24 gave after work andpurification by flash column chromatography [silica (12 g), eluting withEtOAc in hexane 0 to 60%]N-(3-chloro-2-fluorobenzyl)-2-(neopentylamino)acetamide (30a) (200 mg,0.7 mmol, 50% yield) as a clear oil; ¹H NMR (300 MHz, DMSO-d₆) δ 8.55(d, J=5.5 Hz, 1H), 7.79 (t, J=7.5 Hz, 1H), 7.60 (t, J=7.1 Hz, 1H), 7.50(t, J=7.8 Hz, 1H), 4.69 (d, J=5.9 Hz, 2H), 3.44 (s, 2H), 2.90-2.74 (m,2H), 2.41 (s, 1H), 1.16 (d, J=2.9 Hz, 9H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.08; MS (ES+): 287.4 (M+1); (ES−) 285.3 (M−1).

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(neopentyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(30b)

Reaction of N-(3-chloro-2-fluorobenzyl)-2-(neopentylamino)acetamide(30a) (130 mg, 0.45 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (109 mg, 0.5 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by chromatography[silica (12 g), eluting with CMA80 in CHCl₃ 0 to 40%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(neopentyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(30b) (100 mg, 0.21 mmol, 45% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.83 (t, J=5.7 Hz, 1H), 8.18 (d, J=8.1 Hz, 1H), 7.81-7.58 (m,1H), 7.57-7.46 (m, 2H), 7.46-7.31 (m, 3H), 7.30-7.15 (m, 2H), 5.61-5.37(m, 2H), 4.47 (d, J=5.4 Hz, 2H), 4.32 (s, 2H), 3.04 (s, 2H), 1.14-0.71(m, 9H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −120.96; MS (ES+): 488.5 (M+1);(ES−): 486.5 (M−1).

Preparation of(S)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-1-cyclopropyl-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(31d) Step-1: Preparation of (S)-tert-butyl(2-((3-chloro-2-fluorobenzyl)amino)-1-cyclopropyl-2-oxoethyl)carbamate(31b)

Reaction of (S)-2-((tert-butoxycarbonyl)amino)-2-cyclopropylacetic acid(31a) (232 mg, 1.08 mmol, prepared according to method reported byHendricks, Robert Than et al; in U.S. Pat. Appl. Publ., 2011/0230462)with 3-chloro-2-fluorobenzylamine (9d) (172 mg, 1.08 mmol) according tothe procedure reported in step-3 of Scheme 2 gave after workup(5)-tert-butyl(2-((3-chloro-2-fluorobenzyl)amino)-1-cyclopropyl-2-oxoethyl)carbamate(31b) which was used as such in the next step; MS (ES−): 391.3 (M+Cl).

Step-2: Preparation of(S)-2-amino-N-(3-chloro-2-fluorobenzyl)-2-cyclopropylacetamide (31c)

Reaction of (5)-tert-butyl(2-((3-chloro-2-fluorobenzyl)amino)-1-cyclopropyl-2-oxoethyl)carbamate(31b) (378 mg, 1.06 mmol) from above step-1 with TFA (1.5 mL, 19.07mmol) according to the procedure reported in step-2 of Scheme 2 gaveafter workup(S)-2-amino-N-(3-chloro-2-fluorobenzyl)-2-cyclopropylacetamide (31c) TFAsalt which was used in next step without further purification; MS (ES+):257.3 (M+1).

Step-3: Preparation of(S)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-1-cyclopropyl-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(31d)

Reaction of(S)-2-amino-N-(3-chloro-2-fluorobenzyl)-2-cyclopropylacetamide (31c)(272 mg, 1.06 mmol) TFA salt from above step-2 with2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e) (279 mg, 1.27 mmol)according to the procedure reported in step-3 of Scheme 2 gave afterworkup and purification by flash column chromatography [silica gel (24g), eluting with CMA80 in CHCl₃; 0 to 30%](S)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-1-cyclopropyl-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(31d) (21 mg, 0.046 mmol, 4% yield) as an off-white solid; ¹H NMR (300MHz, DMSO-d₆) δ 8.80 (d, J=7.8 Hz, 1H, D₂O exchangeable), 8.62 (t, J=5.8Hz, 1H, D₂O exchangeable), 8.17 (d, J=8.1 Hz, 1H), 7.81-7.60 (m, 2H),7.54-7.36 (m, 3H), 7.32-7.20 (m, 2H), 7.14 (t, J=7.9 Hz, 1H), 5.27 (s,2H), 4.49-4.24 (m, 2H), 3.77 (t, J=8.1 Hz, 1H), 1.17-1.00 (m, 1H),0.59-0.41 (m, 3H), 0.37-0.22 (m, 1H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.16; MS (ES+): 480.5 (M+Na); (ES−): 456.4 (M−1), 492.4 (M+Cl).

Preparation ofN-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-2-(1,3-dioxoisoindolin-2-yl)-N-isopropylacetamide(32b)

To solution of N-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide(19c) (195 mg, 0.75 mmol), N-ethyl-N-isopropylpropan-2-amine (0.66 mL,3.77 mmol), 2-(1,3-dioxoisoindolin-2-yl)acetic acid (32a) (186 mg, 0.9mmol), in DMF (6 mL) was added bromo-tris-pyrrolidinophosphoniumhexafluorophosphate (PyBrop, 422 mg, 0.9 mmol) and stirred atroom temperature for 14 h. The reaction mixture was diluted with brine(100 mL) and extracted with EtOAc (3×100 mL). The organic layers werecombined, dried, filtered and evaporated to dryness. The residueobtained was purified by flash column chromatography [silica gel (24 g),eluting with MeOH in CHCl₃ 0-100%] to affordN-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-2-(1,3-dioxoisoindolin-2-yl)-N-isopropylacetamide(32b) (103 mg, 0.23 mmol, 31% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.73 & 8.34 (2t, J=5.9 Hz, 1H), 7.97-7.82 (m, 4H), 7.55-7.33(m, 2H), 7.28-7.06 (m, 1H), 4.64-4.17 (m, 5H), 4.13 & 3.81 (2s, 2H),1.20 & 0.96 (2d, J=6.6 Hz, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.07,−121.49 (based on NMR the compound is a mixture of two rotamers with˜1:1 ratio); MS (ES+): 446.5 (M+1), 468.4 (M+Na); (ES−) 444.5 (M−1);Analysis calculated for C₂₂H₂₁ClFN₃O₄: C, 59.26; H, 4.75; N, 9.42;Found: C, 58.86; H, 4.84; N, 9.36.

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropylmethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(33b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-((cyclopropylmethyl)amino)acetamide (33a)

Reaction of 2-amino-N-(3-chloro-2-fluorobenzyl)acetamide (16c) (250 mg,1.15 mmol) with cyclopropanecarbaldehyde (89 mg, 1.27 mmol) according tothe procedure reported in step-1 of Scheme 24 gave after workup andpurification by flash column chromatographyN-(3-chloro-2-fluorobenzyl)-2-((cyclopropylmethyl)amino)acetamide (33a)(190 mg, 38% yield); MS (ES+): 271.3 (M+1).

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropylmethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(33b)

Reaction ofN-(3-chloro-2-fluorobenzyl)-2-((cyclopropylmethyl)amino)acetamide (33a)(190 mg, 0.7 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e)(169 mg, 0.77 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup and purification by chromatography [silica(12 g), eluting with CMA80 in CHCl₃ 0 to 60%]1-(2-((2-(3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropylmethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(33b) (41 mg, 0.087 mmol, 12% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) (a mixture of two rotamers) δ 8.96-8.39 (m, 1H), 8.18 (d, J=7.5Hz, 1H), 7.87-7.66 (m, 1H), 7.62-7.03 (m, 7H), 5.54 (2s, 2H), 4.57-3.98(m, 4H), 3.46-3.39 (m, 1H), 3.22-2.99 (m, 1H), 1.22-0.69 (m, 1H),0.62-0.04 (m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −120.74, 121.14; MS(ES+): 472.5 (M+1), 494.5 (M+Na); 470.6 (M−1).

Preparation of1-(2-(((2S,3R)-1-((3-chloro-2-fluorobenzyl)amino)-3-hydroxy-1-oxobutan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(34d) Step-1: Preparation of tert-butyl((2S,3R)-1-((3-chloro-2-fluorobenzyl)amino)-3-hydroxy-1-oxobutan-2-yl)carbamate(34b)

Reaction of (2S,3R)-2-((tert-butoxycarbonyl)amino)-3-hydroxybutanoicacid (34a) (481 mg, 2.19 mmol) with 3-chloro-2-fluorobenzylamine (9d)(350 mg, 2.19 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup tert-butyl((2S,3R)-1-((3-chloro-2-fluorobenzyl)amino)-3-hydroxy-1-oxobutan-2-yl)carbamate(34b) which was used as such in the next step.

Step-2: Preparation of(2S,3R)-2-amino-N-(3-chloro-2-fluorobenzyl)-3-hydroxybutanamide (34c)

Reaction of tert-butyl ((2S,3R)-1-((3-chloro-2-fluorobenzyl)amino)-3-hydroxy-1-oxobutan-2-yl)carbamate(34b) (791 mg, 2.19 mmol) from above step-1 with TFA (3.04 mL, 39.5mmol) according to the procedure reported in step-2 of Scheme 2 gaveafter workup(2S,3R)-2-amino-N-(3-chloro-2-fluorobenzyl)-3-hydroxybutanamide (34c)TFA salt which was used in next step without further purification.

Step-3: Preparation of1-(2-(((2S,3R)-1-((3-chloro-2-fluorobenzyl)amino)-3-hydroxy-1-oxobutan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(34d)

Reaction of(2S,3R)-2-amino-N-(3-chloro-2-fluorobenzyl)-3-hydroxybutanamide (34c)(680 mg, 2.61 mmol) TFA salt from above step-2 with2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e) (572 mg, 2.61 mmol)according to the procedure reported in Scheme 32 gave after workup1-(2-(((2S,3R)-1-((3-chloro-2-fluorobenzyl)amino)-3-hydroxy-1-oxobutan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(34d) (28 mg, 0.061 mmol, 2% yield) as an off-white solid; ¹H NMR (300MHz, DMSO-d₆) δ 8.50 (t, J=5.8 Hz, 1H, D20 exchangeable), 8.39 (d, J=8.3Hz, 1H, D₂O exchangeable), 8.17 (d, J=8.1 Hz, 1H), 7.71 (s, 1H, D₂Oexchangeable), 7.62 (d, J=8.5 Hz, 1H), 7.52-7.36 (m, 3H), 7.34-7.22 (m,2H), 7.18-7.05 (m, 1H), 5.36 (s, 2H), 5.07 (d, J=4.7 Hz, 1H, D₂Oexchangeable), 4.37 (t, J=4.7 Hz, 2H), 4.20 (dd, J=8.3, 3.9 Hz, 1H),4.13-4.02 (m, 1H), 1.07 (d, J=6.2 Hz, 3H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.36; MS (ES+): 484.5 (M+Na); (ES−) 460.5 (M−1), 496.4 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(propyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(35d) Step-1: Preparation of2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b)

To a solution of 2-chloroacetyl chloride (35a) (1.04 g, 9.21 mmol) andtriethylamine (1.93 mL, 13.81 mmol) in THF (10 mL) at 0° C. was added(3-chloro-2-fluorophenyl)methanamine (9d) (1.47 g, 9.21 mmol). Thereaction mixture was stirred at room temperature overnight, quenchedwith water (20 mL) and extracted with DCM (3×20 mL). The organic layerswere combined, dried, filtered and concentrated in vacuum to dryness.The residue obtained was purified by chromatography [silica (24 g),eluting with EtOAc/MeOH (9:1) in hexane 0 to 40%] to afford2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (1.2 g, 5.08 mmol,55% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 8.81 (t, J=5.2Hz, 1H), 7.50 (td, J=7.8, 1.8 Hz, 1H), 7.35-7.26 (m, 1H), 7.25-7.15 (m,1H), 4.37 (d, J=5.8 Hz, 2H), 4.13 (s, 2H); ¹⁹F NMR (282 MHz, DMSO) δ−121.08; MS (ES+) 236.2 (M+1); 234.1 (M−2).

Step-2: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-(propylamino)acetamide (35c)

To a solution of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b)(600 mg, 2.54 mmol) in CH₃CN (10 mL) was added propan-1-amine (300 mg,5.08 mmol), K₂CO₃ (878 mg, 6.35 mmol) and heated at 60° C. for 5 h. Theinorganic solid was removed by filtration and filtrate was concentratedin vacuum to dryness. The residue obtained was purified bychromatography [silica (12 g), eluting with EtOAc/MeOH (9:1) in hexane 0to 60%] to give N-(3-chloro-2-fluorobenzyl)-2-(propylamino)acetamide(35c) (468 mg, 1.81 mmol, 71% yield) as a yellow oil; ¹H NMR (300 MHz,DMSO-d₆) δ 8.35 (t, J=5.9 Hz, 1H), 7.53-7.39 (m, 1H), 7.34-7.22 (m, 1H),7.22-7.11 (m, 1H), 4.37 (d, J=6.0 Hz, 2H), 3.12 (s, 2H), 2.41 (t, J=7.1Hz, 2H), 2.16 (s, 1H), 1.50-1.29 (m, 2H), 0.84 (t, J=7.4 Hz, 3H); ¹⁹FNMR (282 MHz, DMSO) δ −121.68; MS (ES+) 259.4 (M+1); 257.3 (M−1).

Step-3: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(propyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(35d)

Reaction of N-(3-chloro-2-fluorobenzyl)-2-(propylamino)acetamide (35c)(130 mg, 0.50 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e)(121 mg, 0.55 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(propyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(35d) (155 mg, 0.34 mmol, 67% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) (a mixture of two rotamers) δ 8.84 and 8.48 (2t, J=5.8 Hz, 1H),8.23-8.13 (m, 1H), 7.71 (d, J=8.3 Hz, 1H), 7.61-7.03 (m, 7H), 5.56 and5.47 (2s, 2H), 4.46 and 4.33 (2d, J=5.7 Hz, 2H), 4.24 and 3.95 (2s, 2H),3.49-3.38 (m, 1H), 3.25-3.13 (m, 1H), 1.53 (m, 2H), 0.93 and 0.77 (2t,J=7.3 Hz, 3H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.25, 121.63; MS (ES+)482.5 (M+Na); 458.4 (M−1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(ethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(36b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-(ethylamino)acetamide (36a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (600 mg,2.54 mmol) with ethanamine hydrochloride (415 mg, 5.08 mmol) accordingto the procedure reported in step-2 of Scheme 35 gave after workupN-(3-chloro-2-fluorobenzyl)-2-(ethylamino)acetamide (36a) (494 mg, 2.02mmol, 79% yield) as a yellow oil; ¹H NMR (300 MHz, DMSO-d₆) δ 8.39 (t,J=5.8 Hz, 1H), 7.53-7.40 (m, 1H), 7.33-7.23 (m, 1H), 7.23-7.13 (m, 1H),4.37 (d, J=5.9 Hz, 2H), 3.14 (s, 2H), 2.50 (q, J=7.1 Hz, 2H), 2.25 (s,1H), 1.00 (t, J=7.1 Hz, 3H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.72; MS(ES+) 245.3 (M+1); 243.2 (M−1).

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(ethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(36b)

Reaction of N-(3-chloro-2-fluorobenzyl)-2-(ethylamino)acetamide (36a)(174 mg, 0.71 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e)(171 mg, 0.78 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(ethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(36b) (69 mg, 0.156 mmol, 22% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) (a mixture of two rotamers) δ 8.85 and 8.49 (2t, J=5.5 Hz, 1H),8.18 (d, J=8.1 Hz, 1H), 7.71 (d, J=7.4 Hz, 1H), 7.62-7.09 (m, 7H), 5.57and 5.45 (2s, 2H), 4.46 and 4.34 (2d, J=5.5 Hz, 2H), 4.24 and 3.95 (2s,2H), 3.56-3.24 (m, 2H), 1.23 and 0.97 (2t, J=7.1 Hz, 3H); ¹⁹F NMR (282MHz, DMSO-d₆) δ −121.28, 121.65; MS (ES+) 468.5 (M+Na); 444.5 (M−1);[based on NMR, this compound is a mixture of rotamers with 1:1 ratio]

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isobutyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(37b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-(isobutylamino)acetamide (37a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (200 mg,0.85 mmol) with isobutylamine (124 mg, 1.7 mmol), according to theprocedure reported in step-2 of Scheme 35 gave after workupN-(3-chloro-2-fluorobenzyl)-2-(isobutylamino)acetamide (37a) (50 mg,0.18 mmol, 22% yield) as a yellow oil; MS (ES+): 273.4 (M+1); (ES−)271.3 (M−1)

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isobutyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(37b)

Reaction of N-(3-chloro-2-fluorobenzyl)-2-(isobutylamino)acetamide (37a)(54 mg, 0.2 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e)(48 mg, 0.22 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup and purification by column chromatography[silica (12 g), eluting with CMA80 in CHCl₃ from 0 to 40%] to give1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isobutyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(37b) (48 mg, 0.1 mmol, 51% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.84 and 8.48 (2t, J=5.6 Hz, 1H), 8.18 (d, J=8.2 Hz, 1H),7.78-7.65 (m, 1H), 7.59-7.00 (m, 7H), 5.54 and 5.50 (2s, 2H), 4.53-3.86(m, 4H), 3.34-2.97 (m, 2H), 2.10-1.65 (m, 1H), 0.99 and 0.79 (2d, J=6.6Hz, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.22, 121.64; MS (ES+): 474.5(M+1); (ES−): 472.4 (M−1); [based on NMR, this compound is a mixture ofrotamers with 3:2 ratio]

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclobutyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(38b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-(cyclobutylamino)acetamide (38a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (530 mg,2.25 mmol) with cyclobutanamine (319 mg, 4.49 mmol), according to theprocedure reported in step-2 of Scheme 35 gave after workup andpurification by chromatography [silica (12 g), eluting with EtOAc/MeOH(9:1) in hexane 0 to 60%]N-(3-chloro-2-fluorobenzyl)-2-(cyclobutylamino)acetamide (38a) (523 mg,1.93 mmol, 86% yield) as a yellow oil; ¹H NMR (300 MHz, DMSO-d₆) δ 8.33(t, J=5.9 Hz, 1H), 7.52-7.39 (m, 1H), 7.32-7.23 (m, 1H), 7.23-7.14 (m,1H), 4.34 (d, J=6.0 Hz, 2H), 3.18-3.07 (m, 1H), 3.05 (s, 2H), 2.37 (s,1H), 2.11-1.96 (m, 2H), 1.75-1.44 (m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.68; MS (ES+): 271.4 (M+1); (ES−): 269.3 (M−1);

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclobutyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(38b)

Reaction of N-(3-chloro-2-fluorobenzyl)-2-(cyclobutylamino)acetamide(38a) (210 mg, 0.78 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (187 mg, 0.85 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclobutyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(38b) (298 mg, 0.63 mmol, 81% yield) as an off white solid; ¹H NMR (300MHz, DMSO-d₆) δ 8.87 and 8.43 (2t, J=5.8 Hz, 1H), 8.18 (d, J=7.6 Hz,1H), 7.71 (s, 1H), 7.62-7.02 (m, 7H), 5.56 and 5.42 (s, 2H), 4.75-4.50(m, 1H), 4.49-4.02 (m, 4H), 2.30-2.09 (m, 2H), 2.03-1.86 (m, 2H),1.74-1.46 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.23, 121.61; MS(ES+): 494.5 (M+Na); ES(−): 470.4 (M−1); [based on NMR, this compound isa mixture of rotamers with 2:3 ratio].

Preparation of1-(2-((2-(((6-bromopyridin-2-yl)methyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(39f) Step-1: Preparation of ethyl 2-(isopropylamino)acetate (39b)

A stirred solution of propan-2-amine (22.94 mL, 269 mmol) and ethyl2-chloroacetate (39a) (19.21 mL, 180 mmol) in toluene (200 mL) washeated at reflux for 2 h, cooled to room temperature, diluted with brine(300 mL) and with extracted with EtOAc (2×300 mL). The organic layerscombined were, dried, filtered and evaporated to dryness. The residueobtained was purified by flash column chromatography [Silica gel, 80 geluting with EtOAc in hexanes from 0-30%) to afford ethyl2-(isopropylamino)acetate (39b) (18.78 g, 129 mmol, 72% yield) as ayellow semi-solid; MS (ES+): 146.2 (M+1); (ES−) 180.1 (M+Cl).

Step-2: Preparation of ethyl2-(2-(3-carbamoyl-1H-indazol-1-yl)-N-isopropylacetamido)acetate (39c)

Reaction of ethyl 2-(isopropylamino)acetate (39b) (4.42 g, 30.4 mmol)with 2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e) (4.00 g, 18.25mmol) according to the procedure reported in step-3 of Scheme 2 gaveafter workup ethyl2-(2-(3-carbamoyl-1H-indazol-1-yl)-N-isopropylacetamido)acetate (39c) asan dark yellow oil which was used as such in the next step.

Step-3: Preparation of2-(2-(3-carbamoyl-1H-indazol-1-yl)-N-isopropylacetamido)acetic acid(39d)

To a solution of ethyl2-(2-(3-carbamoyl-1H-indazol-1-yl)-N-isopropylacetamido)acetate (39c)(3.00 g, 8.66 mmol) in of acetonitrile (30 mL) at room temperature wasadded sodium hydroxide (0.762 g, 19.05 mmol) in 30 mL of H2O 2O) andstirred overnight. Acetonitrile was removed by evaporation vacuum andthe aqueous layer was basified with 1 N NaOH, washed with ether. Thebasic aqueous layer was acidified with ice-cold 1 N HCl and the solidobtained was collected by filtration, dried in vacuum to afford2-(2-(3-carbamoyl-1H-indazol-1-yl)-N-isopropylacetamido)acetic acid(39d) (1.53 g, 4.81 mmol, 55.5% yield) as a yellow solid; MS (ES+):341.4 (M+Na); (ES−) 317.4 (M−1).

Step-4: Preparation of1-(2-((2-(((6-bromopyridin-2-yl)methyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(39f)

Reaction of2-(2-(3-carbamoyl-1H-indazol-1-yl)-N-isopropylacetamido)acetic acid(39d) (0.15 g, 0.47 mmol) with (6-bromopyridin-2-yl)methanamine (39e)(0.115 g, 0.613 mmol), according to the procedure reported in step-3 ofScheme 2 gave after workup and purification by flash columnchromatography [Silica gel, 24 g eluting with MeOH in CHCl₃ 0-100%)1-(2-((2-(((6-bromopyridin-2-yl)methyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(39f) (65 mg, 0.13 mmol, 28% yield) as an off-white solid, which wasmixture of rotamers from NMR analysis; ¹H NMR (300 MHz, DMSO-d₆) δ 8.92& 8.46 (2t, J=6.1 Hz, 1H), 8.23-8.12 (m, 1H), 7.78-7.18 (m, 8H), 5.59 &5.46 (2s, 2H), 4.63-4.50 (m, 1H), 4.46 (d, J=5.7 Hz) & 4.31 (d, J=6.1Hz) (2d, 2H), 4.25 & 3.85 (2s, 2H), 1.25 (d, J=6.2 Hz) & 1.02 (dd,J=6.8, 2.0 Hz) (d &dd, 6H); ¹H NMR (300 MHz, DMSO-d₆/D₂O) δ 8.17-8.09(m, 1H), 7.69 (t, J=7.7 Hz, 1H), 7.61-7.33 (m, 4H), 7.31-7.16 (m, 1H),5.57 (s) & 5.42 (s) (2s, 2H), 4.59-4.46 (m, 1H), 4.43 (s) & 4.29 (2s,2H), 4.19 (s, 1H), 1.22 (d, J=6.4 Hz) & 1.00 (d, J=6.8 Hz) (2d, 6H); MS(ES+): 487.5, 489.5 (M+2), 509.5, 511.5 (M+Na); (ES−): 485.4, 487.5(M−1), 521.4, 523.4 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorophenyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(40b)

Reaction of2-(2-(3-carbamoyl-1H-indazol-1-yl)-N-isopropylacetamido)acetic acid(39d) (0.15 g, 0.47 mmol) with 3-chloro-2-fluoroaniline (40a) (0.089 g,0.613 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column chromatography[Silica gel, 24 g eluting with MeOH in CHCl₃ 0-30%)1-(2-((2-((3-chloro-2-fluorophenyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(40b) (51 mg, 0.11 mmol, 24% yield) as an off-white solid; ¹H NMR (300MHz, DMSO-d₆) δ 10.34 & 9.86 (2s, 1H), 8.29-8.10 (m, 1H), 8.02-7.51 (m,3H), 7.51-7.06 (m, 5H), 5.63 & 5.48 (s, 2H), 4.79-3.92 (m, 3H), 1.26 (d,J=6.6 Hz) & 1.06 (d, J=6.8 Hz) (2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−126.60; (based on NMR the compound is a mixture of rotamers with ˜2:3ratio); MS (ES+): 446.5 (M+1); MS (ES−): 444.4 (M−1), 480.4 (M+Cl).

Preparation of1-(2-((2-((3-bromo-2-fluorophenyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(41b)

Reaction of2-(2-(3-carbamoyl-1H-indazol-1-yl)-N-isopropylacetamido)acetic acid(39d) (0.15 g, 0.47 mmol) with 3-bromo-2-fluoroaniline (41a) (90 mg,0.47 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column chromatography[Silica gel, 24 g eluting with MeOH in CHCl₃ from 0-100%)1-(2-((2-((3-bromo-2-fluorophenyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(41b) (48 mg, 0.1 mmol, 21% yield) as an off-white solid; ¹H NMR (300MHz, DMSO-d₆) δ 10.34 & 9.85 (2s, 1H), 8.28-7.02 (m, 9H), 5.63 & 5.49(2s, 2H), 4.83-3.91 (m, 3H), 1.26 (d, J=6.5 Hz) 1.06 (d, J=6.9 Hz) (2d,6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −118.22 (d, J=3.7 Hz); (based on NMRthe compound is a mixture of rotamers with ˜2:3 ratio); MS (ES+): 490.4,492.5 (M+2); MS (ES−): 488.3, 490.3 (M−2).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(2-hydroxyethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(42b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-((2-hydroxyethyl)amino)acetamide (42a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (500 mg,2.12 mmol) with 2-aminoethanol (259 mg, 4.24 mmol) according to theprocedure reported in step-2 of Scheme 35 gave after workup andpurification by chromatography [silica (12 g), eluting with EtOAc/MeOH(9:1) in hexane 0 to 60%]N-(3-chloro-2-fluorobenzyl)-2-((2-hydroxyethyl)amino)acetamide (42a)(402 mg, 1.54 mmol, 73% yield) as a clear oil; ¹H NMR (300 MHz, DMSO-d₆)δ 8.45 (t, J=6.0 Hz, 1H), 7.53-7.40 (m, 1H), 7.33-7.23 (m, 1H),7.23-7.11 (m, 1H), 4.54 (s, 1H), 4.36 (d, J=6.0 Hz, 2H), 3.52-3.40 (m,2H), 3.16 (s, 3H), 2.55 (t, J=5.6 Hz, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−73.53 (TFA peak), −121.72; MS (ES+): 261.3 (M+1), 283.3 (M+Na); (ES−):259.3 (M−1).

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(2-hydroxyethyl)amino)-2-oxo ethyl)-1H-indazole-3-carboxamide (42b)

Reaction of N-(3-chloro-2-fluorobenzyl)-2-((2-hydroxyethyl)amino)acetamide (42a) (210 mg, 0.81 mmol) with2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e) (194 mg, 0.89 mmol)according to the procedure reported in step-3 of Scheme 2 gave afterworkup 1-(2-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxo ethyl)(2-hydroxyethyl)amino)-2-oxo ethyl)-1H-indazole-3-carboxamide (42b) (128 mg, 0.28mmol, 34% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 8.87 and8.57 (2t, J=5.8 Hz, 1H), 8.18 (d, J=8.1 Hz, 1H), 7.78-7.64 (m, 1H),7.60-7.00 (m, 7H), 5.66 and 5.43 (2s, 2H), 5.24 and 4.76 2 (2t, J=5.1Hz, 1H), 4.49-4.32 (m, 2H), 4.00 (s, 1H), 3.72-3.55 (m, 3H), 3.51-3.39(m, 1H), 3.34-3.26 (m, 1H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.33,121.63; MS (ES−): 460.5 (M−1); [based on NMR, this compound is a mixtureof two rotamers with 2:5 ratio].

Preparation of2-(6-amino-4-oxo-4,5-dihydro-2H-pyrazolo[3,4-d]pyrimidin-2-yl)-N-(2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)-N-isopropylacetamide(43g) Step-1: Preparation of ethyl3-amino-1-(2-(tert-butoxy)-2-oxoethyl)-1H-pyrazole-4-carboxylate (43c)

To a solution of ethyl 3-amino-1H-pyrazole-4-carboxylate (43a) (5 g,31.6 mmol) and tert-butyl 2-bromoacetate (5.60 mL, 37.9 mmol) in DMF (20mL) was added Potassium carbonate (6.55 g, 47.4 mmol) and stirred atroom temperature overnight. The reaction mixture was diluted with EtOAc(200 mL), washed with water (2×100 mL), brine (100 mL), dried, filteredand concentrated in vacuum. The residue was purified by flash columnchromatography on silica gel eluting with hexanes/EtOAc (1:0 to 2:1) toafford ethyl3-amino-1-(2-(tert-butoxy)-2-oxoethyl)-1H-pyrazole-4-carboxylate (43b)as a (1.16 g, 14%) as a yellow solid; ¹H NMR (300 MHz, DMSO-d₆) δ 7.93(s, 1H), 5.37 (s, 2H), 4.69 (s, 2H), 4.17 (q, J=7.1 Hz, 2H), 1.42 (s,9H), 1.24 (t, J=7.1 Hz, 3H); MS (ES+: 270.4 (M+1) and 292.4 (M+Na); andethyl 5-amino-1-(2-(tert-butoxy)-2-oxoethyl)-1H-pyrazole-4-carboxylate(43c) (1.56 g, 18%) as a brown gum. ¹H NMR (300 MHz, DMSO-d₆) δ 7.45 (s,1H), 6.38 (s, 2H), 4.70 (s, 2H), 4.16 (q, J=7.1 Hz, 2H), 1.41 (s, 9H),1.24 (t, J=7.1 Hz, 3H); MS (ES⁻): 268.3 (M−1) and 304.3 (M+Cl).

Step-2: Preparation of(E)-2-(3-(amino(methoxycarbonylamino)methyleneamino)-4-(ethoxycarbonyl)-1H-pyrazol-1-yl)aceticacid (43e)

A mixture of ethyl3-amino-1-(2-(tert-butoxy)-2-oxoethyl)-1H-pyrazole-4-carboxylate (43b)(571 mg, 2.12 mmol) and(Z)-(methoxycarbonylamino)(methylthio)methylenecarbamic acid methylester (43d) (646 mg) in acetic acid (5 mL) was heated with stirring at100° C. overnight. The reaction mixture was cooled to room temperatureand triturated with CHCl₃ followed by filtration, washing with CHCl₃,and drying under vacuum to afford (E)-2-(3-(amino(methoxycarbonylamino)methyleneamino)-4-(ethoxy carbonyl)-1H-pyrazol-1-yl)aceticacid (43e) (290 mg, 44%) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ11.81 (bs, 1H), 8.34 (s, 1H), 8.07 (s, 1H), 4.97 (s, 2H), 4.28 (q, J=7.1Hz, 2H), 3.54 (s, 3H), 1.30 (t, J=7.1 Hz, 3H); MS (ES+): 314 (M+1),

Step-3: Preparation of (E)-ethyl3-(amino(methoxycarbonylamino)methyleneamino)-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-pyrazole-4-carboxylate(43f)

Reaction of(E)-2-(3-(amino(methoxycarbonylamino)methyleneamino)-4-(ethoxycarbonyl)-1H-pyrazol-1-yl)aceticacid (43e) (80 mg, 0.26 mmol) withN-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide (19c) (79 mg,0.306 mmol) according to the procedure reported in step-3 of Scheme-2gave after workup and purification by flash column chromatography onsilica gel eluting with CHCl₃/MeOH (1:0 to 19:1) to give (E)-ethyl3-(amino(methoxycarbonylamino)methyleneamino)-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-pyrazole-4-carboxylate(43f) (64 mg, 45%) as an off-white solid; ¹H NMR ((300 MHz, DMSO-d₆) (asa mixture of two rotamers): δ 11.60 (s, 1H), 8.75 & 8.33 (2t, 1H), 8.26(s, 1H), 8.22 (s, 1H), 8.06 (d, J=13.5 Hz, 1H), 7.59-7.05 (m, 3H), 5.25& 5.05 (2s, 2H), 4.64-4.50 & 4.17-3.98 (2m, 1H), 4.46-4.22 (m, 4H), 4.07& 3.83 (2s, 2H), 3.54 (s, 3H), 1.35-0.92 (m, 9H); ¹⁹F NMR (282 MHz,DMSO-d₆) δ −121.28, −121.69; MS (ES+): 554.6 (M+1) & 556.6 (M+3); MS(ES−): 588.6 and 590.6 (M+Cl).

Step-4: Preparation of2-(6-amino-4-oxo-4,5-dihydro-2H-pyrazolo[3,4-d]pyrimidin-2-yl)-N-(2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)-N-isopropylacetamide(43g)

To a solution of (E)-ethyl3-(amino(methoxycarbonylamino)methyleneamino)-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-pyrazole-4-carboxylate(43f) (54 mg, 0.097 mmol) in MeOH (8 mL) was added with 1 N aqueoussodium hydroxide (0.49 mL, 0.98 mmol) and refluxed for 2.5 h. Thereaction mixture was cooled to room temperature concentrated in vacuumto remove MeOH, diluted with water (10 mL) and acidified with 4 N HCl.The solid obtained was collected by filtration, dried under vacuum toafford2-(6-amino-4-oxo-4,5-dihydro-2H-pyrazolo[3,4-d]pyrimidin-2-yl)-N-(2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)-N-isopropylacetamide(43g) (15 mg, 34%) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) (amixture of two rotamers) 610.35 & 10.33 (2s, 1H), 8.74 & 8.36 (2t, 1H),8.14 & 8.13 (2s, 1H), 7.60-7.07 (m, 3H), 6.20 (bs, 2H), 5.21 & 5.03 (2s,2H), 4.41 (d, J=5.6 Hz) & 4.33 (d, J=5.7 Hz) (2d, 2H), 4.64-4.48 &4.21-4.05 (2m, 1H), 4.10 & 3.83 (2s, 2H), 1.15 (d, J=6.4 Hz) & 0.97 (d,J=6.8 Hz) (2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.35, −121.73. MS(ES+): 450.5 (M+1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(3-hydroxypropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(44b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-((3-hydroxypropyl)amino)acetamide (44a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (500 mg,2.12 mmol) with 2-aminoethanol (318 mg, 4.24 mmol) according to theprocedure reported in step-2 of Scheme 35 gave after workup andpurification by chromatography [silica (12 g), eluting with EtOAc/MeOH(9:1) in hexane 0 to 60%]N-(3-chloro-2-fluorobenzyl)-2-((3-hydroxypropyl)amino)acetamide (44a)(494 mg, 2.02 mmol, 73% yield) as a clear oil; ¹H NMR (300 MHz, DMSO-d₆)δ 8.38 (t, J=6.1 Hz, 1H), 7.52-7.42 (m, 1H), 7.33-7.23 (m, 1H), 7.19(td, J=7.8, 1.0 Hz, 1H), 4.37 (d, J=5.8 Hz, 2H), 4.14 (s, 1H), 3.45 (t,J=6.3 Hz, 2H), 3.18 (s, 2H), 3.13 (s, 2H), 2.56-2.52 (m, 1H), 1.61-1.49(m, 2H); MS (ES⁺) 275.4 (M+1); MS (ES⁻), 273.3 (M−1).

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(3-hydroxypropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(44b)

Reaction ofN-(3-chloro-2-fluorobenzyl)-2-((3-hydroxypropyl)amino)acetamide (44a)(120 mg, 0.44 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e)(105 mg, 0.48 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(3-hydroxypropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(44b) (59 mg, 0.12 mmol, 28% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) (a mixture of two rotamers) δ 8.86 (t, J=5.5 Hz) & 8.51 (t,J=5.9 Hz) (2t, 1H), 8.18 (d, J=8.1 Hz, 1H), 7.72 (d, J=7.1 Hz, 1H),7.60-7.06 (m, 7H), 5.63 & 5.45 (2s, 2H), 4.82-4.29 (m, 3H), 4.26 & 3.94(2s, 2H), 3.65-3.48 (m, 2H), 3.35-3.23 (m, 2H), 1.89-1.46 (m, 2H); ¹⁹FNMR (282 MHz, DMSO) δ −121.30, 121.64; MS (ES+) 476.5 (M+1); MS (ES⁻),510.5 (M+Cl); HPLC, Rt 4.005 min, 93.5338% [based on NMR, this compoundis a mixture of two rotamers 2:5 ratio].

Preparation of1-(2-(cyclopropyl(2-((2-fluoro-3-methoxyphenyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(45f) Step-1: Preparation of ethyl 2-(cyclopropylamino)acetate (45b)

Reaction of ethyl 2-bromoacetate (45a) (10 g, 59.9 mmol) withcyclopropylamine (16.88 mL, 240 mmol) in ethanol (80 mL) at roomtemperature according to the procedure reported in step-1 of Scheme 39gave after workup ethyl 2-(cyclopropylamino)acetate (45b) (7.2 g, 50.3mmol, 84% yield) as light orange colored liquid; ¹H NMR (300 MHz,DMSO-d₆) δ 4.09 (q, J=7.1 Hz, 2H), 3.30 (s, 2H), 2.60 (s, 1H), 2.23-2.09(m, 1H), 1.19 (t, J=7.1 Hz, 3H), 0.37-0.28 (m, 2H), 0.24-0.17 (m, 2H);MS (ES+) 144.2 (M+1).

Step-2: Preparation of ethyl2-(2-(3-carbamoyl-1H-indazol-1-yl)-N-cyclopropylacetamido)acetate (45c)

Reaction of ethyl 2-(cyclopropylamino)acetate (45b) (1.57 g, 10.95 mmol)with 2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e) (2 g, 9.12 mmol)according to the procedure reported in step-3 of Scheme 2 gave afterworkup ethyl2-(2-(3-carbamoyl-1H-indazol-1-yl)-N-cyclopropylacetamido)acetate (45c)(2 g, 5.81 mmol, 64% yield) as off-white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.22-8.14 (m, 1H), 7.71 (s, 1H), 7.66-7.59 (m, 1H), 7.47-7.35(m, 2H), 7.26 (ddd, J=7.9, 6.9, 0.9 Hz, 1H), 5.69 (s, 2H), 4.16-3.99 (m,4H), 3.15-3.02 (m, 1H), 1.31-1.21 (m, 2H), 1.17 (t, J=7.1 Hz, 3H),1.03-0.88 (m, 2H); MS (ES+): 345.5 (M+1), 367.4 (M+Na), MS (ES−): 379.5(M+Cl).

Step-3: Preparation of2-(2-(3-carbamoyl-1H-indazol-1-yl)-N-cyclopropylacetamido)acetic acid(45d)

Hydrolysis ester of ethyl2-(2-(3-carbamoyl-1H-indazol-1-yl)-N-cyclopropylacetamido)acetate (45c)(1.8 g, 5.23 mmol) according to the procedure reported in step-3 ofScheme 39 gave after workup2-(2-(3-carbamoyl-1H-indazol-1-yl)-N-cyclopropylacetamido)acetic acid(45d) (1.5 g, 4.74 mmol, 91% yield) as light orange colored foam; ¹H NMR(300 MHz, DMSO-d₆) δ 12.76 (s, 1H), 8.18 (dt, J=8.1, 1.0 Hz, 1H), 7.73(s, 1H), 7.64 (dt, J=8.6, 0.9 Hz, 1H), 7.47-7.36 (m, 2H), 7.26 (ddd,J=8.0, 6.8, 0.9 Hz, 1H), 5.68 (s, 2H), 4.00 (s, 2H), 3.12-2.99 (m, 1H),1.06-0.86 (m, 4H).

Step-4: Preparation of1-(2-(cyclopropyl(2-((2-fluoro-3-methoxyphenyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(45f)

Reaction of2-(2-(3-carbamoyl-1H-indazol-1-yl)-N-cyclopropylacetamido)acetic acid(45d) (0.12 g, 0.38 mmol) with 2-fluoro-3-methoxyaniline (0.054 g, 0.379mmol) (45e) (54 mg, 0.379 mmol), according to the procedure reported instep-1 of Scheme 2 gave after workup and purification by flash columnchromatography [Silica gel, 12 g eluting with MeOH/EtOAc (9:1) in hexane0-100%]1-(2-(cyclopropyl(2-((2-fluoro-3-methoxyphenyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(45f) (70 mg, 0.159 mmol, 42% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 9.83 (s, 1H), 8.18 (dt, J=8.1, 1.0 Hz, 1H), 7.74 (s, 1H),7.66 (d, J=8.5 Hz, 1H), 7.59-7.34 (m, 3H), 7.32-7.20 (m, 1H), 7.06 (td,J=8.3, 1.8 Hz, 1H), 6.98-6.86 (m, 1H), 5.70 (s, 2H), 4.20 (s, 2H), 3.82(s, 3H), 3.11 (s, 1H), 1.05-0.91 (m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−147.62; MS (ES+): 440.5 (M+1), 462.5 (M+Na), MS (ES−): 438.5 (M−1).

Preparation of1-(2-(cyclopropyl(2-oxo-2-((3-(trifluoromethoxy)phenyl)amino)ethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(46b)

Reaction of2-(2-(3-carbamoyl-1H-indazol-1-yl)-N-cyclopropylacetamido)acetic acid(45d) (0.12 g, 0.38 mmol) with 23-(trifluoromethoxy)aniline (46a) (67mg, 0.379 mmol) according to the procedure reported in step-1 of Scheme2 gave after workup and purification by flash column chromatography[Silica gel, 12 g eluting with MeOH/EtOAc (9:1) in hexane 0-100%]1-(2-(cyclopropyl(2-oxo-2-((3-(trifluoromethoxy)phenyl)amino)ethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(46b) (65 mg, 0.137 mmol, 36% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 10.38 (s, 1H), 8.22-8.12 (m, 1H), 7.80-7.71 (m, 2H),7.70-7.61 (m, 1H), 7.52-7.33 (m, 4H), 7.30-7.20 (m, 1H), 7.09-6.95 (m,1H), 5.71 (s, 2H), 4.15 (s, 2H), 3.18-3.06 (m, 1H), 1.11-0.89 (m, 4H);¹⁹F NMR (282 MHz, DMSO-d₆) δ −56.72; MS (ES+): 476.5 (M+1), 498.5(M+Na), MS (ES−): 474.5 (M−1).

Preparation of(S)-1-(2-((1-((3-chloro-2-fluorobenzyl)amino)-1-oxopentan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(47d) Step-1: Preparation of (5)-tert-butyl(1-((3-chloro-2-fluorobenzyl)amino)-1-oxopentan-2-yl)carbamate (47b)

Reaction of (S)-2-((tert-butoxycarbonyl)amino)pentanoic acid (47a) (412mg, 1.9 mmol) with 3-chloro-2-fluorobenzylamine (9d) (252 mg, 1.58 mmol)according to the procedure reported in step-3 of Scheme 2 gave afterworkup (5)-tert-butyl(1-((3-chloro-2-fluorobenzyl)amino)-1-oxopentan-2-yl)carbamate (47b)which was used as such in the next step. MS (ES+): 381.45 (M+Na); (ES−):393.34 (M+Cl).

Step-2: Preparation of(S)-2-amino-N-(3-chloro-2-fluorobenzyl)pentanamide (47c)

Reaction of (5)-tert-butyl(1-((3-chloro-2-fluorobenzyl)amino)-1-oxopentan-2-yl)carbamate (47b)(567 mg, 1.58 mmol) with TFA (2.19 mL, 28.4 mmol) according to theprocedure reported in step-2 of Scheme 2 gave after workup(S)-2-amino-N-(3-chloro-2-fluorobenzyl)pentanamide (47c) which was usedas such in the next step; MS (ES+): 259.4 (M+1).

Step-3: Preparation of(S)-1-(2-((1-((3-chloro-2-fluorobenzyl)amino)-1-oxopentan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(47d)

Reaction of (S)-2-amino-N-(3-chloro-2-fluorobenzyl)pentanamide (47c)(409 mg, 1.58 mmol) TFA salt from above step-2 with2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e) (416 mg, 1.9 mmol)according to the procedure reported in step-3 of Scheme 2 gave afterworkup and purification by chromatography [silica (24 g), eluting withMeOH in CHCl₃ from 0 to 50%](5)-1-(2-((1-((3-chloro-2-fluorobenzyl)amino)-1-oxopentan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(47d) (12 mg, 0.026 mmol, 2% yield) as an off-white solid; ¹H NMR (300MHz, DMSO-d₆) δ 8.65 (t, J=5.8 Hz, 1H), 8.59 (d, J=7.9 Hz, 1H), 8.17(dt, J=8.2, 1.1 Hz, 1H), 7.70 (s, 1H), 7.66-7.59 (m, 1H), 7.53-7.37 (m,3H), 7.31-7.21 (m, 2H), 7.19-7.09 (m, 1H), 5.26 (s, 2H), 4.38-4.20 (m,3H), 1.66-1.53 (m, 2H), 1.33-1.26 (m, 2H), 0.86 (t, J=7.4 Hz, 3H); ¹⁹FNMR (282 MHz, DMSO-d₆) δ −121.48; MS (ES+): 460.47 (M+1), 482.5 (M+Na);(ES−): 458.40 (M−1), 494.41 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopentyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(48b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-(cyclopentylamino)acetamide (48a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (500 mg,2.12 mmol) with cyclopentylamine (216 mg, 2.54 mmol) according to theprocedure reported in step-2 of Scheme 35 gave after workup andpurification by chromatography [silica (12 g), eluting with EtOAc/MeOH(9:1) in hexane 0 to 60%]N-(3-chloro-2-fluorobenzyl)-2-(cyclopentylamino)acetamide (48a) as aclear oil which was used as such in next step; MS (ES+): 285.4 (M+1); MS(ES−): 283.3 (M−1).

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopentyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(48b)

Reaction of N-(3-chloro-2-fluorobenzyl)-2-(cyclopentylamino)acetamide(48a) (240 mg, 0.84 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (203 mg, 0.93 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopentyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(48b) (315 mg, 0.65 mmol, 77% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.84 (t, J=5.6 Hz) and 8.40 (t, J=5.8 Hz) (2t, 1H), 8.18 (d,J=8.1 Hz, 1H), 7.71 (s, 1H), 7.64-7.00 (m, 7H), 5.63 & 5.45 (2s, 2H),4.67-4.24 (m, 3H), 4.19 & 3.82 (2s, 2H), 2.06-1.84 (m, 1H), 1.75-1.28(m, 7H); ¹⁹F NMR (282 MHz, DMSO) δ −121.17, 121.71; MS (ES⁺) 486.6(M+1); MS (ES⁻), 484.4 (M−1); HPLC, Rt 7.134 min, 96.7156% [based onNMR, this compound is a mixture of two rotamers 1:1 ratio].

Preparation of1-(2-((2-((6-bromopyrazin-2-yl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(49d) Step-1: Preparation of N-(6-bromopyrazin-2-yl)-2-chloroacetamide(49b)

Reaction of 2-chloroacetyl chloride (35a) (0.24 mL, 3 mmol) with6-bromopyrazin-2-amine (49a) (350 mg, 2.01 mmol) according to theprocedure reported in step-1 of Scheme 35 gave after workupN-(6-bromopyrazin-2-yl)-2-chloroacetamide (49b) (45 mg, 1.8 mmol, 89%yield) as a dark orange solid; ¹H NMR (300 MHz, DMSO-d₆) δ 11.51 (s,1H), 9.28 (d, J=0.6 Hz, 1H), 8.60 (d, J=0.6 Hz, 1H), 4.39 (s, 2H); MS(ES+): 250.2, 252.2 (M, M+2), MS (ES−): 248.1, 250.1 (M−2, M).

Step-2: Preparation ofN-(6-bromopyrazin-2-yl)-2-(cyclopropylamino)acetamide (49c)

Reaction of N-(6-bromopyrazin-2-yl)-2-chloroacetamide (49b) (480 mg,1.92 mmol) with Cyclopropylamine (0.34 mL, 4.79 mmol) according to theprocedure reported in step-2 of Scheme 35 gave after workup andpurification by column chromatography [silica gel (24 g), eluting withEtOAc in hexane 0 to 100%]N-(6-bromopyrazin-2-yl)-2-(cyclopropylamino)acetamide (49c) (33 mg, 1.22mmol, 64% yield) as an orange colored solid; ¹H NMR (300 MHz, DMSO-d₆) δ9.33 (s, 1H), 8.55 (s, 1H), 4.00 (s, 1H), 3.43 (s, 2H), 2.24-2.10 (m,1H), 0.41-0.30 (m, 2H), 0.29-0.18 (m, 2H); MS (ES−): 269.2, 271.2 (M−2,M).

Step-3: Preparation of1-(2-((2-((6-bromopyrazin-2-yl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(49d)

Reaction of N-(6-bromopyrazin-2-yl)-2-(cyclopropylamino)acetamide (49c)(90 mg, 0.33 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e)(73 mg, 0.33 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup1-(2-((2-((6-bromopyrazin-2-yl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(49d) (110 mg, 0.23 mmol, 70% yield) as white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 11.29 (s, 1H), 9.25 (s, 1H), 8.54 (s, 1H), 8.17 (d, J=8.2,1H), 7.72 (s, 1H), 7.69-7.64 (m, 1H), 7.50-7.34 (m, 2H), 7.25 (d, J=7.9,1H), 5.71 (s, 2H), 4.22 (s, 2H), 3.20-3.06 (m, 1H), 1.14-0.84 (m, 4H);MS (ES+): 472.4, 474.5 (M+1, M+3), MS (ES−): 470.4, 472.4.

Preparation of1-(2-((3-((6-bromopyridin-2-yl)amino)-3-oxopropyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(50d) Step-1: Preparation of 3-bromo-N-(6-bromopyridin-2-yl)propanamide(50b)

Reaction of 3-bromopropanoyl chloride (50a) (1g, 5.83 mmol) with6-bromopyridin-2-amine (2b) (1.01 g, 5.83 mmol) according to theprocedure reported in step-1 of Scheme 35 gave after workup andpurification by flash column chromatography [silica (24 g), eluting withEtOAc/MeOH (9:1) in hexane 0 to 40%] to give3-bromo-N-(6-bromopyridin-2-yl)propanamide (50b) (1.26 g, 4.09 mmol,70.1% yield) as a white solid; MS (ES+): 307.2 (M+1).

Step-2: Preparation ofN-(6-bromopyridin-2-yl)-3-(isopropylamino)propanamide (50c)

Reaction of 3-bromo-N-(6-bromopyridin-2-yl)propanamide (50b) (520 mg,1.69 mmol) with propan-2-amine (299 mg, 5.07 mmol) according to theprocedure reported in step-2 of Scheme 35 gave after workup andpurification by flash column chromatography [silica (12 g), eluting withEtOAc/MeOH (9:1) in hexane 0 to 60%]N-(6-bromopyridin-2-yl)-3-(isopropylamino)propanamide (50c) (321 mg,1.12 mmol, 66% yield) as a clear oil; MS (ES+): 286.3 (M+1); MS (ES−):284.3 (M−1).

Step-3: Preparation of1-(2-((3-((6-bromopyridin-2-yl)amino)-3-oxopropyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(50d)

Reaction of N-(6-bromopyridin-2-yl)-3-(isopropylamino)propanamide (50c)(230 mg, 0.8 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e)(194 mg, 0.88 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with CMA80 in CHCl₃ 0 to 40%]1-(2-((3-((6-bromopyridin-2-yl)amino)-3-oxopropyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(50d) (325 mg, 0.67 mmol, 83% yield) as an off white solid; ¹H NMR (300MHz, DMSO-d₆) δ 11.06 & 10.82 (2s, 1H), 8.28-7.99 (m, 2H), 7.86-7.54 (m,3H), 7.49-7.20 (m, 4H), 5.60 & 5.55 (2s, 2H), 4.41-4.12 (m, 1H), 3.71(t, J=7.1 Hz) & 3.48-3.40 (M) (t & m, 2H), 2.90 (t, J=7.1 Hz) &2.63-2.60 (m) (t & m, 2H), 1.25 (d, J=6.5 Hz) & 1.15 (d, J=6.8 Hz) (2d,6H); MS (ES+): 487.4 (M+1); [based on NMR, this compound is a mixture oftwo rotamers with 4:5 ratio].

Preparation of methyl2-(2-(3-carbamoyl-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)acetamido)acetate(51b) Step-1: Preparation of methyl2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)acetate (51a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (500 mg,2.12 mmol) with methyl 2-aminoacetate (266 mg, 2.12 mmol) according tothe procedure reported in step-2 of Scheme 35 gave after workup andpurification by flash column chromatography [silica (12 g), eluting withEtOAc/MeOH (9:1) in hexane 0 to 60%] methyl2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)acetate (51a)(293 mg, 1.02 mmol, 48% yield) as a clear oil; MS (ES+) 311.3 (M+Na)

Step-2: Preparation of2-(2-(3-carbamoyl-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)acetamido)acetate(51b)

Reaction of methyl2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)acetate (51a)(200 mg, 0.69 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e)(167 mg, 0.76 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with CMA80 in CHCl₃ 0 to 60%]2-(2-(3-carbamoyl-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)acetamido)acetate(51b) (36 mg, 0.073 mmol, 11% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.82 (t, J=5.8 Hz) and 8.53 (t, J=5.3 Hz) (2t, 1H), 8.18 (d,J=7.5 Hz, 1H), 7.74 (s, 1H), 7.52-7.09 (m, 7H), 5.54 and 5.51 (2s, 2H),4.57-4.28 (m, 4H), 4.08 and 3.99 (2s, 2H), 3.75 and 3.61 (2s, 3H); ¹⁹FNMR (282 MHz, DMSO) δ −121.32, −121.61; MS (ES+): 490.5 (M+1), 512.5(M+Na); MS (ES−): 488.4 (M−1); [based on NMR, this compound is a mixtureof two rotamers with 5:4 ratio].

Preparation of tert-butyl3-(2-(3-carbamoyl-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)acetamido)azetidine-1-carboxylate(52b) Step-1: Preparation of tert-butyl3-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)azetidine-1-carboxylate(52a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (925 mg,3.92 mmol) with tert-butyl 3-aminoazetidine-1-carboxylate (710 mg, 4.12mmol) according to the procedure reported in step-2 of Scheme 35 gaveafter workup and purification by flash column chromatography [silica (12g), eluting with EtOAc/MeOH (9:1) in hexane 0 to 60%] tert-butyl3-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)azetidine-1-carboxylate(52a) (785 mg, 2.11 mmol, 51% yield) as a clear oil; MS (ES+) 372.4(M+1); MS (ES−): 370.4 (M−1).

Step-2: Preparation of tert-butyl3-(2-(3-carbamoyl-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)acetamido)azetidine-1-carboxylate(52b)

Reaction of tert-butyl3-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)azetidine-1-carboxylate(52a) (440 mg, 1.18 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (285 mg, 1.3 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with CMA80 in CHCl₃ 0 to 60%]tert-butyl3-(2-(3-carbamoyl-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)acetamido)azetidine-1-carboxylate(52b) (325 mg, 0.57 mmol, 48% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.93 (t, J=5.6 Hz) and 8.59 (t, J=5.8 Hz) (2t, 1H), 8.18 (d,J=8.1 Hz, 1H), 7.69 (d, J=8.7 Hz, 1H), 7.59-7.02 (m, 7H), 5.60 & 5.43(2s, 2H), 5.12-4.74 (m, 1H), 4.48 (d, J=5.4 Hz) & 4.33 (d, J=5.6 Hz)(2d, 2H), 4.39 & 4.10 (2s, 2H), 4.16 (t, J=8.7 Hz) & 4.01-3.76 (m) (t &m, 4H), 1.39 & 1.35 (2s, 9H); ¹⁹F NMR (282 MHz, DMSO) δ −121.26, 121.61;MS (ES+) 573.7 (M+1); [based on NMR, this compound is a mixture of tworotamers 1:1 ratio].

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(2-fluoroethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(53b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-((2-fluoroethyl)amino)acetamide (53a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (500 mg,2.12 mmol) with tert-fluoroethanamine hydrochloride (422 mg, 4.24 mmol)according to the procedure reported in step-2 of Scheme 35 gave afterworkup and purification by flash column chromatography [silica (12 g),eluting with EtOAc/MeOH (9:1) in hexane 0 to 60%]N-(3-chloro-2-fluorobenzyl)-2-((2-fluoroethyl)amino)acetamide (53a) (224mg, 0.85 mmol, 40% yield) as a clear oil; ¹H NMR (300 MHz, DMSO-d₆) δ8.39 (t, J=5.9 Hz, 1H), 7.53-7.44 (m, 1H), 7.31-7.23 (m, 1H), 7.23-7.13(m, 1H), 4.60-4.50 (m, 1H), 4.41-4.32 (m, 3H), 3.19 (s, 2H), 2.82 (t,J=5.0 Hz, 1H), 2.72 (t, J=5.0 Hz, 1H), 2.47-2.37 (m, 1H); ¹⁹F NMR (282MHz, DMSO) δ −121.69; MS (ES+) 263.4 (M+1); 261.3 (M−1);

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(2-fluoroethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(53b)

Reaction ofN-(3-chloro-2-fluorobenzyl)-2-((2-fluoroethyl)amino)acetamide (53a) (178mg, 0.68 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e) (163mg, 0.745 mmol) according to the procedure reported in step-3 of Scheme2 gave after workup and purification by flash column chromatography[silica (12 g), eluting with CMA80 in CHCl₃ 0 to 60%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(2-fluoroethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(53b) (162 mg, 0.349 mmol, 51.5% yield) as a white solid; ¹H NMR (300MHz, DMSO-d₆) δ 8.84 (t, J=5.7 Hz) and 8.54 (t, J=5.8 Hz) (2t, 1H), 8.18(d, J=7.5 Hz, 1H), 7.74 (s, 1H), 7.57-7.07 (m, 7H), 5.59 & 5.48 (2s,2H), 4.88-4.62 (m, 1H), 4.61-4.29 (m, 3H), 4.35 & 4.03 (2s, 2H),3.97-3.80 (m, 1H), 3.62 (t, J=4.8 Hz) and 3.53 (t, J=4.9 Hz) (2t, 1H);MS (ES+): 464.5 (M+1); MS (ES−), 462.4 (M−1); [based on NMR, thiscompound is a mixture of two rotamers with 1:1 ratio].

Preparation of1-(2-((2-(((6-chloropyridin-2-yl)methyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(54b)

Reaction of2-(2-(3-carbamoyl-1H-indazol-1-yl)-N-isopropylacetamido)acetic acid(39d) (0.15 g, 0.47 mmol) with (6-chloropyridin-2-yl)methanamine (54a)(122 mg, 0.57 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup and purification by flash columnchromatography [Silica gel, 24 g eluting with MeOH in CHCl₃ from 0-50%)1-(2-((2-(((6-chloropyridin-2-yl)methyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(54b)_(101 mg, 0.23 mmol, 48% yield) as an off-white solid; ¹H NMR (300MHz, DMSO-d₆) δ 8.93 (t, J=6.0 Hz) & 8.47 (t, J=6.1 Hz) (2t, 1H),8.22-8.13 (m, 1H), 7.85 (t, J=7.8 Hz, 1H), 7.69 (d, J=4.4 Hz, 1H), 7.61(d, J=7.9 Hz, 1H), 7.53 (dt, J=8.5, 1.0 Hz, 1H), 7.46-7.30 (m, 3H),7.31-7.16 (m, 1H), 5.60 & 5.47 (2s, 2H), 4.62-4.50 (m, 1H), 4.47 (d,J=5.8 Hz & 4.32 (d, J=6.0 Hz) (2d, 2H), 4.23 & 3.86 (2s, 2H), 1.25 (d,J=6.5 Hz) & 1.02 (d, J=6.8 Hz) (2d, 6H); (based on NMR the compound is amixture of two rotamers ˜1:2 ratio); MS (ES+): 443.5 (M+1), 465.5(M+Na); (ES−): 441.4 (M−1), 477.4 (M+Cl).

Preparation of1-(2-(cyclopropyl(2-((6-(dimethylamino)pyridin-2-yl)-amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(55a)

To a solution of1-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(7d) (105 mg, 0.22 mmol) in dioxane (1 mL) was added aqueousdimethylamine (0.56 mL, 4.46 mmol) and heated under microwaveirradiation at 150° C. for 3h. The reaction mixture was cooled to roomtemperature, diluted with water (50 mL) and extracted with EtOAc (2×40mL). The organic layers were combined washed with brine, dried, filteredand concentrated in vacuum. The residue obtained was purified bychromatography [silica gel (12 g), eluting with EtOAc/MeOH (9:1) inhexane 0 to 100%] to afford1-(2-(cyclopropyl(2-((6-(dimethylamino)pyridin-2-yl)-amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(55a) (55 mg, 0.13 mmol, 57% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 10.00 (s, 1H), 8.21-8.11 (m, 1H), 7.76 (s, 1H), 7.66 (d,J=8.5 Hz, 1H), 7.52-7.34 (m, 3H), 7.30-7.15 (m, 2H), 6.31 (d, J=8.3 Hz,1H), 5.70 (s, 2H), 4.19 (s, 2H), 3.17-3.05 (m, 1H), 2.98 (s, 6H),1.08-0.86 (m, 4H); MS (ES+): 436.6 (M+1); (ES−): 470.5 (M+Cl).

Preparation of2-(4-amino-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-N-(2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)-N-cyclopropylacetamide(56d) Step-1: Preparation of tert-butyl2-(4-chloro-7H-pyrrolo[2,3-d]pyrimidin-7-yl)acetate (56b)

Reaction of 4-chloro-7H-pyrrolo[2,3-d]pyrimidine (56a) (1.5 g, 9.77mmol) in acetonitrile (60 mL) with tert-butyl 2-bromoacetate (2.16 mL,14.65 mmol) using Potassium carbonate (2.7 g, 19.54 mmol) as baseaccording to the procedure reported step-2 of Scheme 35 gave afterworkup and purification by flash column chromatography [silica gel (40g), eluting with EtOAc in hexanes 0 to 50%] tert-butyl2-(4-chloro-7H-pyrrolo[2,3-d]pyrimidin-7-yl)acetate (56b) (2.2 g, 8.22mmol, 84% yield) as white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 8.65 (s,1H), 7.75 (d, J=3.6 Hz, 1H), 6.68 (d, J=3.6 Hz, 1H), 5.09 (s, 2H), 1.41(s, 9H); MS (ES+) 268.4 (M+1), MS (ES−) 302.3 (M+Cl).

Step-2: Preparation of 2-(4-amino-7H-pyrrolo[2,3-d]pyrimidin-7-yl)aceticacid (56c)

Reaction of tert-butyl2-(4-chloro-7H-pyrrolo[2,3-d]pyrimidin-7-yl)acetate (56b) (512 mg, 1.91mmol) with aqueous conc. ammonium hydroxide (1.5 mL, 38.3 mmol) undermicro irradiation according to the procedure reported Scheme 55 gaveafter workup 2-(4-amino-7H-pyrrolo[2,3-d]pyrimidin-7-yl)acetic acid(56c) (312 mg, 1.62 mmol, 85% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 7.98 (s, 1H), 7.02 (d, J=3.4 Hz, 1H), 6.82 (s, 2H), 6.43 (d,J=3.5 Hz, 1H), 4.45 (s, 2H); MS (ES+): 193.2 (M+1); (ES−): 191.2 (M−1).

Step-3: Preparation of2-(4-amino-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-N-(2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)-N-cyclopropylacetamide(56d)

Reaction of N-(6-bromopyridin-2-yl)-2-(cyclopropylamino)acetamide (7c)(8 mg, 0.3 mmol) with 2-(4-amino-7H-pyrrolo[2,3-d]pyrimidin-7-yl)aceticacid (56c) (57 mg, 0.3 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by chromatography[silica (12 g), eluting with CMA80 in CHCl₃ 0 to 40%]2-(4-amino-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-N-(2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)-N-cyclopropylacetamide(56d) (22 mg, 0.05 mmol, 17% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 10.93 (s, 1H), 8.07-7.95 (m, 2H), 7.72 (t, J=8.0 Hz, 1H),7.32 (d, J=7.7, 0.7 Hz, 1H), 7.07 (d, J=3.5 Hz, 1H), 6.95 (s, 2H), 6.51(d, J=3.5 Hz, 1H), 5.27 (s, 2H), 4.16 (s, 2H), 3.11-2.95 (m, 1H),1.02-0.85 (m, 4H); MS (ES+): 444.5, 446.4 (M+1, M+3), MS (ES−): 442.3,444.4.

Preparation ofN-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-2-(4-chloro-5-cyano-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-N-isopropylacetamide(57d) Step-1: Preparation of tert-butyl2-(4-chloro-5-cyano-7H-pyrrolo[2,3-d]pyrimidin-7-yl)acetate (57b)

To a solution of 4-chloro-7H-pyrrolo[2,3-d]pyrimidine-5-carbonitrile(57a) (811 mg, 4.54 mmol) in DMF (10 mL) was added at room temperature,NaH (60% in mineral oil, 218 mg, 5.45 mmol) stirred for 5 mins followedby the addition of tert-butyl 2-bromoacetate (0.81 mL, 5.45 mmol). Thereaction mixture was stirred for 2 h quenched with EtOAc (50 mL) andbrine (75 mL). The organic layer was separated washed with water (50mL), dried, filtered and concentrated in vacuum. The residue obtainedwas purified by flash column chromatography [silica gel (24 g), elutingwith MeOH in CHCl₃ 0 to 30%] to afford tert-butyl2-(4-chloro-5-cyano-7H-pyrrolo[2,3-d]pyrimidin-7-yl)acetate (57b) (989mg, 3.38 mmol, 74% yield) as an off-white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.86 (s, 1H), 8.71 (s, 1H), 5.18 (s, 2H), 1.42 (s, 9H); MS(ES+): 293.4 (M+1), 315.3 (M+Na); (ES−): 291.3 (M−1), 327.4 (M+Cl).

Step-2: Preparation of2-(4-chloro-5-cyano-7H-pyrrolo[2,3-d]pyrimidin-7-yl)acetic acid (57c)

Reaction of tert-butyl2-(4-chloro-5-cyano-7H-pyrrolo[2,3-d]pyrimidin-7-yl)acetate (57b) (500mg, 1.71 mmol) with TFA (1.32 mL, 17.08 mmol) according to the procedurereported in step-2 of Scheme 2 gave after workup2-(4-chloro-5-cyano-7H-pyrrolo[2,3-d]pyrimidin-7-yl)acetic acid (57c)(310 mg, 1.31 mmol, 77% yield) which was used as such in the next stepwithout further purification; MS (ES+): 237.3 (M+1); (ES−): 235.2 (M−1)

Step-3: Preparation ofN-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-2-(4-chloro-5-cyano-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-N-isopropylacetamide(57d)

Reaction of N-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide(19c) (387 mg, 1.5 mmol) with2-(4-chloro-5-cyano-7H-pyrrolo[2,3-d]pyrimidin-7-yl)acetic acid (57c)(295 mg, 1.25 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup and purification by chromatography [Firstcolumn: Silica gel (24 g), eluting with MeOH in CHCl₃ 0-100%; Secondcolumn: Silica gel (24 g) eluting with EtOAc/MeOH (9:1) in hexanes0-100%;)N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-2-(4-chloro-5-cyano-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-N-isopropylacetamide(57d) (115 mg, 0.241 mmol, 19% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.82 & 8.82 (2s, 1H), 8.79 & 8.33 (2t, 1H), 8.64 & 8.61 (2s,1H), 7.57-7.33 (m, 2H), 7.30-7.03 (m, 1H), 5.46 & 5.33 (2s, 2H),4.62-4.47 & 4.26-4.20 (2m, 1H), 4.44 (d, J=5.6 Hz) & 4.30 (d, J=5.8 Hz)(2d, 2H), 4.18 & 3.84 (2s, 2H), 1.24 (d, J=6.4 Hz) & 0.98 (d, J=6.8 Hz)(2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.27, −121.63; [based on NMRthe compound is a mixture of two rotamers ˜2:3 ratio]; MS (ES+): 477.5(M+1); (ES−): 475.5, 477.5 (M−1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(3,3-difluorocyclobutyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(58b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-((3,3-difluorocyclobutyl)amino)acetamide(58a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (500 mg,2.12 mmol) with 3,3-difluorocyclobutanamine hydrochloride (502 mg, 3.49mmol) according to the procedure reported in step-2 of Scheme 35 gaveafter workup and purification by flash column chromatography [silica (12g), eluting with EtOAc/MeOH (9:1) in hexane 0 to 60%]N-(3-chloro-2-fluorobenzyl)-2-((3,3-difluorocyclobutyl)amino)acetamide(58a) (110 mg, 0.36 mmol, 17%) as a clear oil; ¹H NMR (300 MHz, DMSO-d₆)δ 8.39 (t, J=6.0 Hz, 1H), 7.52-7.43 (m, 1H), 7.33-7.24 (m, 1H),7.24-7.14 (m, 1H), 4.35 (d, J=5.9 Hz, 2H), 3.17-3.03 (m, 3H), 2.80-2.61(m, 3H), 2.41-2.22 (m, 2H); MS (ES+): 307.3, 309.3 (M+1, M+3)

Step-2: Preparation of tert-butyl1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(3,3-difluorocyclobutyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(58b)

Reaction ofN-(3-chloro-2-fluorobenzyl)-2-((3,3-difluorocyclobutyl)amino)acetamide(58a) (110 mg, 0.36 mmol,) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (86 mg, 0.4 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with CMA80 in CHCl₃ 0 to 60%]tert-butyl1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(3,3-difluorocyclobutyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(58b) (115 mg, 0.23 mmol, 63% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.90 (t, J=5.9 Hz) and 8.57 (t, J=6.6 Hz) (2t, 1H), 8.18 (d,J=8.0 Hz, 1H), 7.79-7.63 (m, 1H), 7.56-7.07 (m, 7H), 5.65 and 5.43 (2s,2H), 4.64-4.02 (m, 5H), 3.12-2.85 (m, 2H), 2.80-2.65 (m, 2H); ¹⁹F NMR(282 MHz, DMSO-d₆) δ −82.66, −99.20, −121.23, −121.60; MS (ES⁻¹): 508.5(M+1); MS (ES⁻): 506.5 (M−1); [based on NMR, this compound is a mixtureof two rotamers 5:1 ratio].

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(2-hydroxy-2-methylpropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(59b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-((2-hydroxy-2-methylpropyl)amino)acetamide(59a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (500 mg,2.12 mmol) with 1-amino-2-methylpropan-2-ol (378 mg, 4.24 mmol)according to the procedure reported in step-2 of Scheme 35 gave afterworkup and purification by flash column chromatography [silica (12 g),eluting with EtOAc/MeOH (9:1) in hexane 0 to 60%]N-(3-chloro-2-fluorobenzyl)-2-((2-hydroxy-2-methylpropyl)amino)acetamide(59a) (200 mg, 0.69 mmol, 33%) as a clear oil; MS (ES+) 289.4 (M+1);(ES−) 287.3.

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(2-hydroxy-2-methylpropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(59b)

Reaction ofN-(3-chloro-2-fluorobenzyl)-2-((2-hydroxy-2-methylpropyl)amino)acetamide(59a) (200 mg, 0.69 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (167 mg, 0.76 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with CMA80 in CHCl₃ 0 to 60%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(2-hydroxy-2-methylpropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(59b) (239 mg, 0.49 mmol, 70% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.83 (t, J=5.6 Hz and 8.49 (t, J=5.9 Hz) (2t, 1H), 8.18 (d,J=8.1 Hz, 1H), 7.71 (d, J=11.8 Hz, 1H), 7.57-7.01 (m, 7H), 5.69 and 5.44(2s, 2H), 5.08 and 4.59 (2s, 1H), 4.52-4.28 (m, 3H), 4.07 (s, 1H), 3.50and 3.20 (2s, 2H), 1.24 and 1.03 (2s, 6H); ¹⁹F NMR (282 MHz, DMSO) δ−121.34, −121.67; MS (ES+): 490.5 (M+1); MS (ES−): 488.5 (M−1); [basedon NMR, this compound is a mixture of two rotamers with 1:1 ratio].

Preparation of2-(4-amino-5-cyano-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(60a)

To a solution ofN-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-2-(4-chloro-5-cyano-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-N-isopropylacetamide(57d) (80 mg, 0.17 mmol) in dioxane (3 mL) was added aqueous ammoniumhydroxide (1.83 mL, 46.9 mmol) and heated at 85° C. for 18 h. Thereaction was cooled to room temperature and excess solvent was removedunder reduced pressure. The residue obtained was triturated with CHCl₃and the solid obtained was collected by filtration, rinsed with MeOH,evaporated to dryness to afford2-(4-amino-5-cyano-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(60a) (36 mg, 0.079 mmol, 47% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.77 (t, J=5.8 Hz) and 8.31 (t, J=5.9 Hz) (2t, 1H), 8.18 and8.18 (2s, 1H), 8.07 and 8.06 (2s, 1H), 7.57-7.33 (m, 2H), 7.28-7.06 (m,1H), 6.84 (s, 2H), 5.25 and 5.12 (2s, 2H), 4.63-4.48 and 4.26-4.19 (2m,1H), 4.43 (d, J=5.6 Hz) and 4.31 (d, J=5.8 Hz) (2d, 2H), 4.15 and 3.83(2s, 2H), 1.21 (d, J=6.4 Hz) and 0.97 (d, J=6.8 Hz) (2d, 6H); ¹⁹F NMR(282 MHz, DMSO-d₆) δ −121.31, −121.67. [based on NMR the compound is amixture of two rotamers 1:1 ratio]; MS (ES+): 458.5 (M+1), 480.5 (M+Na);(ES−): 456.4 (M−1), 492.5 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(3-fluoropropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(61b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-((3-fluoropropyl)amino)acetamide (61a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (494 mg,2.09 mmol) with 3-fluoropropan-1-amine hydrochloride (250 mg, 2.201mmol) according to the procedure reported in step-2 of Scheme 35 gaveafter workup and purification by flash column chromatography [silica (12g), eluting with EtOAc/MeOH (9:1) in hexane 0 to 60%]N-(3-chloro-2-fluorobenzyl)-2-((3-fluoropropyl)amino)acetamide (61a)(287 mg, 1.04 mmol, 47%) as a clear oil; MS (ES+): 277.4, 279.3 (M+1,M+3); (ES−): 275.3

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(3-fluoropropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(61b)

Reaction ofN-(3-chloro-2-fluorobenzyl)-2-((3-fluoropropyl)amino)acetamide (61a)(144 mg, 0.52 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e)(125 mg, 0.57 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with CMA80 in CHCl₃ 0 to 60%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(3-fluoropropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(61b) (145 mg, 0.30 mmol, 58% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.87 (t, J=5.7 Hz) and 8.52 (t, J=5.9 Hz) (2t, 1H), 8.18 (d,J=8.1 Hz, 1H), 7.78-7.66 (m, 1H), 7.61-7.07 (m, 7H), 5.58 and 5.45 (2s,2H), 4.70 and 4.54 (2t, J=5.6 Hz, 1H), 4.51-4.30 (m, 3H), 4.27 and 3.97(2s, 2H), 3.62 (t, J=7.1 Hz) and 3.39-3.33 (t & m, 2H), 2.17-1.96 and1.90-1.68 (2m, 2H); ¹⁹F NMR (282 MHz, DMSO) δ −121.27, −121.62; MS (ES+)478.5 (M+1); MS (ES−), 476.5 (M−1); [based on NMR, this compound is amixture of two rotamers with 5:4 ratio].

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(oxetan-3-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(62b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-(oxetan-3-ylamino)acetamide (62a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (500 mg,2.12 mmol) with oxetan-3-amine (310 mg, 4.24 mmol) according to theprocedure reported in step-2 of Scheme 35 gave after workup andpurification by flash column chromatography [silica (12 g), eluting withEtOAc/MeOH (9:1) in hexane 0 to 60%]N-(3-chloro-2-fluorobenzyl)-2-(oxetan-3-ylamino)acetamide (62a) (365 mg,1.34 mmol, 63% yield) as a yellow oil; MS (ES+) 273.3, 275.3 (M+1, M+3);(ES−): 271.3 (M−1)

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(oxetan-3-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(62b)

Reaction of N-(3-chloro-2-fluorobenzyl)-2-(oxetan-3-ylamino)acetamide(62a) (200 mg, 0.73 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (177 mg, 0.81 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with CMA80 in CHCl₃ 0 to 60%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(oxetan-3-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(62b) (192 mg, 0.41 mmol, 55% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.94 (t, J=5.7 Hz) and 8.59 (t, J=5.8 Hz) (2t, 1H), 8.17 (d,J=8.2 Hz, 1H), 7.68 (d, J=14.5 Hz, 1H), 7.57-7.05 (m, 7H), 5.58 and 5.44(2s, 2H), 5.12 (t, J=7.4 Hz, 1H), 4.80 (t, J=7.2 Hz) and 4.69 (t, J=6.7Hz (2t, 2H), 4.58 (t, J=7.2 Hz, 1H), 4.54-4.45 (m, 2H), 4.43 and 4.24(2s, 2H), 4.34 (d, J=5.6 Hz, 1H); ¹⁹F NMR (282 MHz, DMSO) δ −121.26,−121.67; MS (ES+): 474.5 (M+1); MS (ES−): 472.4 (M−1); [based on NMR,this compound is a mixture of two rotamers with 5:4 ratio].

Preparation of2-(4-amino-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(63a)

Reaction of N-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide(10b) (85 mg, 0.33 mmol) with2-(4-amino-7H-pyrrolo[2,3-d]pyrimidin-7-yl)acetic acid (56c) (64 mg,0.33 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by chromatography [silica (12 g),eluting with CMA80 in CHCl₃ 0 to 40%]2-(4-amino-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(63a) (42 mg, 0.097 mmol, 29% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.44 (t, J=5.9 Hz, 1H), 8.01 (s, 1H), 7.47 (td, J=7.6, 1.8Hz, 1H), 7.28-7.19 (m, 1H), 7.15 (td, J=7.8, 1.0 Hz, 1H), 7.06 (d, J=3.5Hz, 1H), 6.96 (s, 2H), 6.52 (d, J=3.5 Hz, 1H), 5.25 (s, 2H), 4.33 (d,J=5.7 Hz, 2H), 3.96 (s, 2H), 3.07-2.94 (m, 1H), 1.01-0.82 (m, 4H); ¹⁹FNMR (282 MHz, DMSO-d₆) δ −121.62; MS (ES+): 431.5 & 433.4 (M+1), MS(ES−): 429.5 (M−1).

Preparation of1-(2-(azetidin-3-yl(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(64b)

Reaction of tert-butyl3-(2-(3-carbamoyl-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)acetamido)azetidine-1-carboxylate(52b) (236 mg, 0.41 mmol) with TFA (0.19 mL, 2.47 mmol) according to theprocedure reported in step-2 of Scheme 2 gave after workup andpurification by chromatography [silica (12 g), eluting with CMA80 inCHCl₃ 0 to 60%]1-(2-(azetidin-3-yl(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(64b) (112 mg, 0.24 mmol, 58% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.94 (t, J=5.7 Hz) and 8.51 (t, J=6.0 Hz) (2t, 1H), 8.17 (d,J=8.2 Hz, 1H), 7.68 (bs, 1H), 7.52-7.22 (m, 7H), 5.55 and 5.41 (2s, 2H),4.91 (m, 1H), 4.47 (d, J=5.3 Hz) and 4.33 (d, J=5.5 Hz) (2d, 2H), 4.42and 4.18 (2s, 2H), 3.62 (d, J=7.2 Hz, 2H), 3.41 (d, J=7.6 Hz, 2H), 3.35(s, 1H); ¹⁹F NMR (282 MHz, DMSO) δ −121.28, −121.64; MS (ES+) 473.5(M+1); MS (ES−), 471.4 (M−1); [based on NMR, this compound is a mixtureof two rotamers 1:1 ratio].

Preparation of4-amino-7-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carboxamide(65a)

To a solution of2-(4-amino-5-cyano-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(60a) (32 mg, 0.07 mmol) in ethanol (5 mL) was added aq. ammoniumhydroxide (0.54 mL, 13.98 mmol) followed by aq. hydrogen peroxide (35%,0.122 mL, 1.398 mmol) and stirred at room temperature for 16 h. Excesssolvent was removed under reduced pressure and the residue obtained waspurified by flash column chromatography [Silica gel (12 g), eluting withMeOH in CHCl₃ 0-50%) to afford4-amino-7-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carboxamide(65a) (14 mg, 0.029 mmol, 42% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.79 (t, J=5.7 Hz) and 8.35 (t, J=5.9 Hz) (2t, 1H), 8.04 and8.04 (2s, 1H), 7.90 and 7.88 (2s, 1H), 7.58-7.35 (m, 2H), 7.34-7.07 (m,3H), 5.21 and 5.08 (2s, 2H), 4.63-4.51 and 4.28-4.23 (2m, 1H), 4.43 (d,J=5.6 Hz) and 4.31 (d, J=5.8 Hz) (2d, 2H), 4.17 and 3.84 (2s, 2H), 1.20(d, J=6.4 Hz) and 0.97 (d, J=6.8 Hz) (2d, 6H); ¹⁹F NMR (282 MHz,DMSO-d₆) δ −121.32, −121.70. [based on NMR the compound is a mixture oftwo rotamers 1:1 ratio]; MS (ES+): 476.5 (M+1), 498.5 (M+Na); (ES−):474.5 (M−1), 510.3 (M+Cl).

Preparation of2-(4-amino-1H-pyrazolo[3,4-d]pyrimidin-1-yl)-N-(2-((6-bromopyrazin-2-yl)amino)-2-oxoethyl)-N-cyclopropylacetamide(66d) Step-1: Preparation of tert-butyl2-(4-chloro-1H-pyrazolo[3,4-d]pyrimidin-1-yl)acetate (66b)

Reaction of 4-chloro-1H-pyrazolo[3,4-d]pyrimidine (66a) (6.82 g, 44.16mmol) with tert-butyl 2-bromoacetate (7.82 mL, 52.96 mmol) usingpotassium carbonate (9.14 g, 66.13 mmol) as base according to theprocedure reported step-2 of Scheme 35 gave after workup andpurification by flash column chromatography [silica gel (40 g), elutingwith EtOAc in hexanes 0 to 60%] tert-butyl2-(4-chloro-1H-pyrazolo[3,4-d]pyrimidin-1-yl)acetate (66b) (4.5 g, 16.75mmol, 38% yield) as white solid.

Step-2: Preparation of2-(4-amino-1H-pyrazolo[3,4-d]pyrimidin-1-yl)acetic acid (66c)

A solution of tert-butyl2-(4-chloro-1H-pyrazolo[3,4-d]pyrimidin-1-yl)acetate (66b) (300 mg, 1.12mmol) in methanolic ammonia (3.72 mL, 11.16 mmol) was stirred at roomtemperature for 2d, concentrated in vacuum and the residue was purifiedby chromatography [silica gel (12 g), eluting with EtOAc/MeOH (9:1) inhexanes 0 to 100%] afforded intermediate product. This material wasdissolved in DCM (5 mL), added TFA (0.86 mL, 11.16 mmol) and stirred atroom temperature for 4d. The solvent was removed under vacuum andresultant residue was suspended in toluene (10 mL) and evaporated. Thesolid was dried under vacuum to afford2-(4-amino-1H-pyrazolo[3,4-d]pyrimidin-1-yl)acetic acid (66c) (0.14 g,0.73 mmol, 65% yield) as an off-white solid; ¹H NMR (300 MHz, DMSO-d₆) δ9.24 (s, 1H), 8.64 (s, 1H), 8.39 (s, 1H), 8.32 (s, 1H), 5.16 (s, 2H); MS(ES+) 194.2 (M+1).

Step-3: Preparation of2-(4-amino-1H-pyrazolo[3,4-d]pyrimidin-1-yl)-N-(2-((6-bromopyrazin-2-yl)amino)-2-oxoethyl)-N-cyclopropylacetamide(66d)

Reaction of N-(6-bromopyrazin-2-yl)-2-(cyclopropylamino)acetamide (49c)(70 mg, 0.26 mmol) with2-(4-amino-1H-pyrazolo[3,4-d]pyrimidin-1-yl)acetic acid (66c) (50 mg,0.26 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by chromatography [silica (12 g),eluting with CMA80 in CHCl₃ 0 to 40%]2-(4-amino-1H-pyrazolo[3,4-d]pyrimidin-1-yl)-N-(2-((6-bromopyrazin-2-yl)amino)-2-oxoethyl)-N-cyclopropylacetamide(66d) (62 mg, 0.14 mmol, 54% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 11.27 (s, 1H), 9.25 (s, 1H), 8.54 (s, 1H), 8.15 (s, 1H), 8.08(s, 1H), 7.87-7.54 (m, 2H), 5.45 (s, 2H), 4.19 (s, 2H), 3.14-3.02 (m,1H), 1.02-0.88 (m, 4H); MS (ES+): 446.4 & 448.4 (M+1), 468.4 & 470.4(M+Na).

Preparation of2-(4-amino-1H-pyrazolo[3,4-d]pyrimidin-1-yl)-N-(2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)-N-cyclopropylacetamide(67a)

Reaction of N-(6-bromopyrazin-2-yl)-2-(cyclopropylamino)acetamide (7c)(70 mg, 0.26 mmol) with2-(4-amino-1H-pyrazolo[3,4-d]pyrimidin-1-yl)acetic acid (66c) (50 mg,0.26 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by chromatography [silica (12 g),eluting with CMA80 in CHCl₃ 0 to 40%]2-(4-amino-1H-pyrazolo[3,4-d]pyrimidin-1-yl)-N-(2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)-N-cyclopropylacetamide(67a) (68 mg, 0.153 mmol, 59% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 10.93 (s, 1H), 8.15 (s, 1H), 8.08 (s, 1H), 8.02 (d, J=8.1 Hz,1H), 7.86-7.53 (m, 3H), 7.33 (dd, J=7.7, 0.7 Hz, 1H), 5.43 (s, 2H), 4.15(s, 2H), 3.12-3.00 (m, 1H), 1.01-0.86 (m, 4H); MS (ES+); 445.4 & 447.4(M+1), 467.4 & 469.5 (M+Na), MS (ES−): 443.4 & 445.4 (M−1).

Preparation of2-(4-amino-1H-pyrazolo[3,4-d]pyrimidin-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(68a)

Reaction of N-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide(10b) (70 mg, 0.27 mmol) with2-(4-amino-1H-pyrazolo[3,4-d]pyrimidin-1-yl)acetic acid (66c) (53 mg,0.27 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by chromatography [silica (12 g),eluting with CMA80 in CHCl₃ 0 to 40%]2-(4-amino-1H-pyrazolo[3,4-d]pyrimidin-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(68a) (85 mg, 0.2 mmol, 72% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.45 (t, J=5.8 Hz, 1H), 8.14 (s, 1H), 8.08 (s, 1H), 7.88-7.52(m, 2H), 7.47 (td, J=7.6, 1.8 Hz, 1H), 7.27-7.19 (m, 1H), 7.19-7.10 (m,1H), 5.42 (s, 2H), 4.32 (d, J=5.7 Hz, 2H), 3.95 (s, 2H), 3.09-2.95 (m,1H), 0.99-0.82 (m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.62; MS (ES+):432.5 & 433.5 (M+1), 454.4 (M+23), MS (ES−): 430.4 & 432.4 (M−1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(methyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(69d) Step-1: Preparation of2-bromo-N-(3-chloro-2-fluorobenzyl)acetamide (69b)

Reaction of 2-bromoacetic acid (69a) (2.09 g, 15.04 mmol) with3-chloro-2-fluorobenzylamine (9d) (2.0 g, 12.53 mmol) according to theprocedure reported in Scheme 32 gave after workup and purification byflash column chromatography [silica gel (40 g), eluting with EtOAc inhexanes 0-100%] 2-bromo-N-(3-chloro-2-fluorobenzyl)acetamide (69b) (2.58g, 9.21 mmol, 74% yield) as a yellow solid; ¹H NMR (300 MHz, DMSO-d₆) δ8.86 (t, J=5.9 Hz, 1H, D₂O exchangeable), 7.51 (ddd, J=7.9, 7.2, 1.8 Hz,1H), 7.36-7.27 (m, 1H), 7.26-7.16 (m, 1H), 4.44-4.27 (m, 2H), 3.91 (s,2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.04; MS (ES+): 280.2, 282.2 (M+2);(ES−): 278.2, 280.2 (M−2).

Step-2: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-(methylamino)acetamide (69c)

Reaction of 2-bromo-N-(3-chloro-2-fluorobenzyl)acetamide (69b) (300 mg,1.07 mmol) with methylamine (2M in MeOH) (0.962 mL, 1.925 mmol) inethanol (20 mL) according to the procedure reported in step-2 of Scheme35 gave after workupN-(3-chloro-2-fluorobenzyl)-2-(methylamino)acetamide (69c) (217 mg, 0.94mmol, 88% yield) as a yellow oil which was used as such in the nextstep; MS (ES−): 229.2 (M−1).

Step-3: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(methyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(69d)

Reaction of N-(3-chloro-2-fluorobenzyl)-2-(methylamino)acetamide (69c)(217 mg, 0.94 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e)(572 mg, 2.61 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup and purification by flash columnchromatography [Silica gel (24 g), eluting with MeOH in CHCl₃ 0-50%)1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(methyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide (69d) (139mg, 34% yield) as a pale yellow solid; ¹H NMR (300 MHz, DMSO-d₆) δ8.93-8.78 & 8.59-8.45 (2m, 1H), 8.18 (d, J=8.1 Hz, 1H), 7.79-7.58 (m,2H), 7.58-7.33 (m, 3H), 7.34-7.05 (m, 3H), 5.57 & 5.44 (2s, 2H), 4.46(d, J=5.1 Hz) & 4.35 (d, J=5.6 Hz) (2d, 2H), 4.25 & 4.00 (2s, 2H), 3.19& 2.81 (s, 3H)¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.40, −121.64 [based onNMR the compound is a mixture of two rotamers ˜2:3 ratio]; MS (ES+):432.5 (M+1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(4-hydroxybutan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(70b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-((4-hydroxybutan-2-yl)amino)acetamide(70a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (494 mg,2.09 mmol) with 3-aminobutan-1-ol (378 mg, 4.24 mmol) according to theprocedure reported in step-2 of Scheme 35 gave after workup andpurification by flash column chromatography [silica (12 g), eluting withEtOAc/MeOH (9:1) in hexane 0 to 60%]N-(3-chloro-2-fluorobenzyl)-2-((4-hydroxybutan-2-yl)amino)acetamide(70a) (200 mg, 0.69 mmol, 33%) as a clear oil; MS (ES+) 289.4 (M+1);(ES−) 287.3 (M−1).

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(4-hydroxybutan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(70b)

Reaction ofN-(3-chloro-2-fluorobenzyl)-2-((4-hydroxybutan-2-yl)amino)acetamide(70a) (200 mg, 0.69 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (167 mg, 0.76 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with CMA80 in CHCl₃ 0 to 60%]followed by prep-HPLC [C₁₈ column, MeOH in water 0-100%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(4-hydroxybutan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(70b) (102 mg, 0.21 mmol, 30% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.83 (t, J=5.5 Hz) and 8.40 (t, J=5.8 Hz) (2t, 1H), 8.18 (d,J=7.9 Hz, 1H), 7.72 (d, J=6.5 Hz, 1H), 7.58-7.00 (m, 7H), 5.79-5.40 (m,2H), 4.57-3.41 (m, 7H) 3.31 (t, J=6.5 Hz, 1H), 1.80-1.41 (m, 2H), 1.25(d, J=6.5 Hz) & 0.98 (d, J=6.8 Hz) (2d, 3H); ¹⁹F NMR (282 MHz, DMSO) δ−74.30 (TFA peak), −121.26, −121.77; MS (ES⁺) 490.5 (M+1); MS (ES⁻),488.4 (M−1); [based on NMR, this compound is a mixture of two rotamers4:5 ratio].

Preparation of1-(2-(sec-butyl(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(71b) Step-1: Preparation of2-(sec-butylamino)-N-(3-chloro-2-fluorobenzyl)acetamide (71a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (500 mg,2.12 mmol) with butan-2-amine (775 mg, 10.59 mmol) according to theprocedure reported in step-2 of Scheme 35 gave after workup andpurification by flash column chromatography [silica (12 g), eluting withEtOAc/MeOH (9:1) in hexane 0 to 60%]2-(sec-butylamino)-N-(3-chloro-2-fluorobenzyl)acetamide (71a) (170 mg,0.62 mmol, 29%) as a yellow oil; MS (ES+): 273.4 (M+1); MS (ES−): 271.3(M−1).

Step-2: Preparation of1-(2-(sec-butyl(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(71b)

Reaction of 2-(sec-butylamino)-N-(3-chloro-2-fluorobenzyl)acetamide(71a) (170 mg, 0.62 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (150 mg, 0.69 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with CMA80 in CHCl₃ 0 to 60%]1-(2-(sec-butyl(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(71b)_(178 mg, 0.38 mmol, 60% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.82 (t, J=5.7 Hz) and 8.36 (t, J=5.9 Hz) (2t, 1H), 8.18 (d,J=8.1 Hz, 1H), 7.77-7.67 (m, 1H), 7.60-7.02 (m, 7H), 5.66-5.39 (m, 2H),4.57-3.71 (m, 5H), 1.69-1.28 (m, 2H), 1.26-0.61 (m, 6H); ¹⁹F NMR (282MHz, DMSO-d₆) δ −121.19, −121.76; MS (ES+) 474.5 (M+1); MS (ES⁻), 472.5(M−1); [based on NMR, this compound is a mixture of two rotamers 2:1ratio].

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(2-hydroxycyclopentyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(72b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-((2-hydroxycyclopentyl)amino)acetamide(72a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (350 mg,1.48 mmol) with 2-aminocyclopentanol (375 mg, 3.71 mmol) according tothe procedure reported in step-2 of Scheme 35 gave after workup andpurification by flash column chromatography [silica (12 g), eluting withEtOAc/MeOH (9:1) in hexane 0 to 60%]N-(3-chloro-2-fluorobenzyl)-2-((2-hydroxycyclopentyl)amino)acetamide(72a) (158 mg, 0.53 mmol, 36%) as a yellow oil; MS (ES+): 301.3; (ES−):299.3 (M−1).

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(2-hydroxycyclopentyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(72b)

Reaction ofN-(3-chloro-2-fluorobenzyl)-2-((2-hydroxycyclopentyl)amino)acetamide(72a) (158 mg, 0.53 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (127 mg, 0.58 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with CMA80 in CHCl₃ 0 to 60%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(2-hydroxycyclopentyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(72b) (128 mg, 0.26 mmol, 49% yield) as an off white solid; ¹H NMR (300MHz, DMSO-d₆) δ 8.87 (t, J=5.7 Hz) and 8.47 (t, J=5.9 Hz) (2t, 1H), 8.18(d, J=8.1 Hz, 1H), 7.77-7.64 (m, 1H), 7.60-6.99 (m, 7H), 5.69 and 5.43(2s, 1H), 5.36 (d, J=4.7 Hz) and 4.75 (d, J=4.8 Hz) (2d, 2H), 4.50-3.70(m, 6H), 2.04-1.28 (m, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.22,−121.68; MS (ES+) 502.6 (M+1); MS (ES⁻): 500.5 (M−1); [based on NMR,this compound is a mixture of two rotamers 1:3 ratio].

Preparation of(R)-1-(2-(sec-butyl(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(73b) Step-1: Preparation of(R)-2-(sec-butylamino)-N-(3-chloro-2-fluorobenzyl)acetamide (73a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (200 mg,0.85 mmol) with (R)-butan-2-amine (155 mg, 2.12 mmol) according to theprocedure reported in step-2 of Scheme 35 gave after workup andpurification by flash column chromatography [silica (12 g), eluting withEtOAc/MeOH (9:1) in hexane 0 to 60%](R)-2-(sec-butylamino)-N-(3-chloro-2-fluorobenzyl)acetamide (73a) (100mg, 0.37 mmol, 43%) as a yellow oil; MS (ES+): 273.3 (M+1); MS (ES−):271.3 (M−1).

Step-2: Preparation of(R)-1-(2-(sec-butyl(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(73b)

Reaction of (R)-2-(sec-butylamino)-N-(3-chloro-2-fluorobenzyl)acetamide(73a) (100 mg, 0.37 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (88 mg, 0.4 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with CMA80 in CHCl₃ 0 to 60%](R)-1-(2-(sec-butyl(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxo ethyl)-1H-indazole-3-carboxamide (73b) (101 mg, 0.21mmol, 58% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 8.82 (t,J=5.5 Hz) and 8.36 (t, J=5.7 Hz) (2t, 1H), 8.19 (d, J=8.1 Hz, 1H),7.82-7.65 (m, 1H), 7.59-7.01 (m, 7H), 5.68-5.39 (m, 2H), 4.55-3.71 (m,5H), 1.67-1.28 (m, 2H), 1.26-0.65 (m, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.19, −121.76; MS (ES+) 474.6 (M+1); 496.5 (M+Na); MS (ES−), 472.5(M−1); [based on NMR, this compound is a mixture of rotamers 1:3 ratio].

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((1R,2R)-2-hydroxycyclopentyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(74b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-(((1R,2R)-2-hydroxycyclopentyl)amino)acetamide(74a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (350 mg,1.48 mmol) with (1R,2R)-2-aminocyclopentanol (510 mg, 3.71 mmol)according to the procedure reported in step-2 of Scheme 35 gave afterworkup and purification by flash column chromatography [silica (12 g),eluting with EtOAc/MeOH (9:1) in hexane 0 to 60%]N-(3-chloro-2-fluorobenzyl)-2-(((1R,2R)-2-hydroxycyclopentyl)amino)acetamide(74a) (312 mg, 1.04 mmol, 70%) as a yellow oil; MS (ES+): 301.3 (M+1);MS (ES−): 299.3 (M−1).

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((1R,2R)-2-hydroxycyclopentyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(74b)

Reaction ofN-(3-chloro-2-fluorobenzyl)-2-(((1R,2R)-2-hydroxycyclopentyl)amino)acetamide(74a) (135 mg, 0.55 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (132 mg, 0.6 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with CMA80 in CHCl₃ 0 to 60%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((1R,2R)-2-hydroxycyclopentyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(74b) (95 mg, 0.189 mmol, 34.5% yield) as a white solid; ¹H NMR (300MHz, DMSO-d₆) δ 8.87 (t, J=5.8 Hz) and 8.47 (t, J=5.9 Hz) (2t, 1H), 8.18(d, J=8.1 Hz, 1H), 7.71 (d, J=6.5 Hz, 1H), 7.58-7.00 (m, 7H), 5.69 and5.43 (2s, 2H), 5.37 (d, J=4.7 Hz) and 4.76 (d, J=4.8 Hz) (2d, 1H),4.52-3.71 (m, 6H), 2.03-1.37 (m, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.22, −121.68; MS (ES+) 502.6 (M+1); 524.5 (M+Na); [based on NMR,this compound is a mixture of two rotamers 2:7 ratio].

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((1S,2S)-2-hydroxycyclopentyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(75b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-(((1S,2S)-2-hydroxycyclopentyl)amino)acetamide(75a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (350 mg,1.48 mmol) with (1S,2S)-2-aminocyclopentanol (510 mg, 3.71 mmol)according to the procedure reported in step-2 of Scheme 35 gave afterworkup and purification by flash column chromatography [silica (12 g),eluting with EtOAc/MeOH (9:1) in hexane 0 to 60%]N-(3-chloro-2-fluorobenzyl)-2-(((1S,2S)-2-hydroxycyclopentyl)amino)acetamide(75a) (285 mg, 0.95 mmol, 64%) as a yellow oil; MS (ES+): 301.4 (M+1);MS (ES−): 299.4 (M−1).

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((1S,2S)-2-hydroxycyclopentyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(75b)

Reaction ofN-(3-chloro-2-fluorobenzyl)-2-(((1S,2S)-2-hydroxycyclopentyl)amino)acetamide(75a) (165 mg, 0.55 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (132 mg, 0.6 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with CMA80 in CHCl₃ 0 to 60%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((1S,2S)-2-hydroxycyclopentyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(75b) (185 mg, 0.369 mmol, 67.2% yield) as a white solid; ¹H NMR (300MHz, DMSO-d₆) δ 8.88 (t, J=5.6 Hz) and 8.48 (t, J=5.7 Hz) (2s, 1H), 8.18(d, J=8.1 Hz, 1H), 7.78-7.63 (m, 1H), 7.57-6.99 (m, 7H), 5.69 and 5.44(2s, 2H), 5.37 (d, J=4.6 Hz) and 4.76 (d, J=4.7 Hz) (2d, 1H), 4.51-3.72(m, 6H), 2.03-1.45 (m, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.21,−121.67; MS (ES+): 524.5 (M+Na); (ES−): 500.5 (M−1); [based on NMR, thiscompound is a mixture of two rotamers 2:7 ratio].

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclohexyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(76b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-(cyclohexylamino)acetamide (76a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (400 mg,1.69 mmol) with cyclohexanamine (840 mg, 8.87 mmol) according to theprocedure reported in step-2 of Scheme 35 gave after workup andpurification by flash column chromatography [silica (12 g), eluting withEtOAc/MeOH (9:1) in hexane 0 to 60%]N-(3-chloro-2-fluorobenzyl)-2-(cyclohexylamino)acetamide (76a) (331 mg,1.11 mmol, 65%) as a yellow oil; MS (ES+): 299.4 (M+1); MS (ES−): 297.3(M−1).

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclohexyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(76b)

Reaction of N-(3-chloro-2-fluorobenzyl)-2-(cyclohexylamino)acetamide(76a) (145 mg, 0.49 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (117 mg, 0.53 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with CMA80 in CHCl₃ 0 to 60%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclohexyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(76b) (176 mg, 0.352 mmol, 72.5% yield) as a white solid; ¹H NMR (300MHz, DMSO-d₆) δ 8.82 (t, J=5.7 Hz) and 8.33 (t, J=5.8 Hz) (2t, 1H), 8.18(d, J=8.1 Hz, 1H), 7.76-7.65 (m, 1H), 7.64-7.02 (m, 7H), 5.60 and 5.47(2s, 2H), 4.46 (d, J=5.5 Hz) and 4.32 (d, J=5.7 Hz) (2d, 2H), 4.24-3.70(m, 3H), 1.90-0.93 (m, 10H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.11,−121.68; MS (ES+): 500.5 (M+1); MS (ES−): 498.5 (M−1); [based on NMR,this compound is a mixture of two rotamers with 1:1 ratio].

Preparation of1-(2-(tert-butyl(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(77b) Step-1: Preparation of2-(tert-butylamino)-N-(3-chloro-2-fluorobenzyl)acetamide (77a)

Reaction of 2-bromo-N-(3-chloro-2-fluorobenzyl)acetamide (69b) (300 mg,1.07 mmol) with 2-methylpropan-2-amine (0.2 mL, 1.93 mmol) according tothe procedure reported in step-2 of Scheme 35 gave after workup2-(tert-butylamino)-N-(3-chloro-2-fluorobenzyl)acetamide (77a) (226 mg,0.83 mmol, 77%) as a yellow oil which was used as such without furtherpurification; ¹H NMR (300 MHz, DMSO-d₆) δ 8.38 (t, J=5.9 Hz, 1H),7.51-7.43 (m, 1H), 7.30-7.23 (m, 1H), 7.22-7.15 (m, 1H), 4.36 (d, J=6.1Hz, 2H), 3.09 (s, 2H), 2.28 (s, 1H), 1.00 (s, 9H); ¹⁹F NMR (282 MHz,DMSO-d₆) δ −121.72; MS (ES+): 273.4 (M+1); MS (ES−): 271.3 (M−1).

Step-2: Preparation of1-(2-(tert-butyl(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(77b)

Reaction of 2-(tert-butylamino)-N-(3-chloro-2-fluorobenzyl)acetamide(77a) (210 mg, 0.77 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (203 mg, 0.92 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with MeOH in CHCl₃ 0 to 50%]1-(2-(tert-butyl(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(77b) (37 mg, 0.078 mmol, 10% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.81 (t, J=5.7 Hz, 1H, D₂O exchangeable), 8.18 (dt, J=8.3,1.0 Hz, 1H), 7.76 (s, 1H, D₂O exchangeable), 7.60-7.48 (m, 2H),7.47-7.33 (m, 3H), 7.31-7.16 (m, 2H), 5.39 (s, 2H), 4.47 (d, J=5.5 Hz,2H), 4.25 (s, 2H), 1.29 (s, 9H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.23;MS (ES+): 474.5 (M+1), 496.4 (M+Na); MS (ES−): 508.6 (M+Cl).

Preparation of1-(2-(cyclopropyl(2-oxo-2-((6-vinylpyridin-2-yl)amino)ethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(78a)

To a degassed solution of1-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(170 mg, 0.36 mmol) in dioxane (5 mL) was added potassiumvinyltrifluoroborate (97 mg, 0.72 mmol), tetrakistriphenylphosphinePalladium (0) (42 mg, 0.036 mmol), degassed solution of potassiumcarbonate (100 mg, 0.72 mmol) in water (0.5 mL). The reaction mixturewas stirred under argon atmosphere for 16 h, quenched with water (30 mL)and EtOAc (40 mL). The organic layers was separated and aqueous layerwas extracted with EtOAc (20 mL). The organic layers were combinedwashed with brine, dried, filtered and concentrated in vacuum. Theresidue was purified by flash column chromatography [silica gel (12 g),eluting with EtOAc-MeOH (9:1) in hexane 0 to 100%] to afford1-(2-(cyclopropyl(2-oxo-2-((6-vinylpyridin-2-yl)amino)ethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(78a) (80 mg, 0.191 mmol, 53% yield) as an off-white solid; ¹H NMR (300MHz, DMSO-d₆) δ 10.57 (s, 1H), 8.17 (d, J=8.1 Hz, 1H), 7.91 (d, J=8.2Hz, 1H), 7.81-7.70 (m, 2H), 7.67 (d, J=8.5 Hz, 1H), 7.50-7.33 (m, 2H),7.31-7.13 (m, 2H), 6.72 (dd, J=17.4, 10.8 Hz, 1H), 6.19 (dd, J=17.5, 1.8Hz, 1H), 5.70 (s, 2H), 5.46 (dd, J=10.7, 1.7 Hz, 1H), 4.21 (s, 2H),3.20-3.05 (m, 1H), 1.10-0.84 (m, 4H); MS (ES+): 419.5 (M+1); (ES−)453.4.5 (M+Cl).

Preparation of1-(2-(cyclopropyl(2-((6-ethylpyridin-2-yl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(79a)

A solution of1-(2-(cyclopropyl(2-oxo-2-((6-vinylpyridin-2-yl)amino)ethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(78a) (35 mg, 0.084 mmol) in EtOAc (5 mL) containing PdOH₂ (12 mg, 0.084mmol) was hydrogenated at atmospheric pressure for 16 h. The reactionmixture was filtered over a Celite pad to remove catalyst and filtratewas concentrated in vacuum. The residue was purified by flashchromatography [silica gel (4 g), eluting with CMA80 in CHCl₃ 0 to 40%]to afford1-(2-(cyclopropyl(2-((6-ethylpyridin-2-yl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(79a) (18 mg, 0.043 mmol, 51% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 10.53 (s, 1H), 8.17 (d, J=8.1, 1.0 Hz, 1H), 7.83 (d, J=8.5Hz, 1H), 7.76 (s, 1H), 7.72-7.62 (m, 2H), 7.48-7.35 (m, 2H), 7.30-7.20(m, 1H), 6.96 (d, J=7.5 Hz, 1H), 5.70 (s, 2H), 4.19 (s, 2H), 3.17-3.05(m, 1H), 2.65 (q, J=7.6 Hz, 2H), 1.19 (t, J=7.6 Hz, 3H), 1.07-0.87 (m,4H); MS (ES+): 421.5 (M+1); (ES−): 419.5 (M−1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(2,2-dimethylcyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(80b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-((2,2-dimethylcyclopropyl)amino)acetamide(80a)

Reaction of 2-bromo-N-(3-chloro-2-fluorobenzyl)acetamide (69b) (300 mg,1.07 mmol) with 2,2-dimethylcyclopropanamine (182 mg, 2.14 mmol)according to the procedure reported in step-2 of Scheme 35 gave afterworkupN-(3-chloro-2-fluorobenzyl)-2-((2,2-dimethylcyclopropyl)amino)acetamide(80a) (305 mg, 1.07 mmol, 100%) as a yellow oil which was used as suchwithout further purification; MS (ES+): 285.4 (M+1); MS (ES−): 283.3(M−1).

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(2,2-dimethylcyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(80b)

Reaction ofN-(3-chloro-2-fluorobenzyl)-2-((2,2-dimethylcyclopropyl)amino)acetamide(80a) (305 mg, 1.07 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (282 mg, 1.29 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (24 g), eluting with MeOH in CHCl₃ 0 to 50%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(2,2-dimethylcyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(80b) (68 mg, 0.14 mmol, 1% yield) as a white solid in the form ofmixture of two rotamers; ¹H NMR (300 MHz, DMSO-d₆) (a mixture of tworotamers) δ 8.83 (J=5.7 Hz) & 8.50 (J=5.8 Hz (2t, 1H), 8.22-8.16 (m,1H), 7.73 & 7.70 (2s, 1H), 7.58-7.36 (m, 4H), 7.32-7.19 (m, 2H), 7.11(td, J=7.8, 1.0 Hz, 1H), 5.74-5.25 (m, 2H), 4.37-4.30 (m, 2H), 4.17-3.81(m, 2H), 2.96 (dd, J=8.0, 4.5 Hz, 1H), 1.28 & 0.96 (2s, 3H), 1.18 & 0.91(2s, 3H), 0.87-0.74 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.23,−121.56; MS (ES+): 486.5 (M+1), 508.5 (M+Na); MS (ES−): 484.5 (M−1),520.5 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(tetrahydrofuran-3-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(81b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-((tetrahydrofuran-3-yl)amino)acetamide(81a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (300 mg,1.27 mmol) with tetrahydrofuran-3-amine (332 mg, 3.81 mmol) according tothe procedure reported in step-2 of Scheme 35 gave after workup andpurification by flash column chromatography [silica (12 g), eluting withEtOAc/MeOH (9:1) in hexane 0 to 60%]N-(3-chloro-2-fluorobenzyl)-2-((tetrahydrofuran-3-yl)amino)acetamide(81a) (152 mg, 0.53 mmol, 42% yield) as a clear oil; ¹H NMR (300 MHz,DMSO-d₆) δ ¹H NMR (300 MHz, DMSO-d₆) δ 8.37 (t, J=6.0 Hz, 1H, D₂Oexchangeable), 7.48 (td, J=7.8, 1.8 Hz, 1H), 7.33-7.24 (m, 1H),7.24-7.12 (m, 1H), 4.36 (d, J=6.0 Hz, 2H), 3.83-3.55 (m, 3H), 3.46-3.36(m, 1H), 3.30-3.18 (m, 1H), 3.14 (s, 2H), 2.35 (s, 1H, D₂Oexchangeable), 1.95-1.80 (m, 1H), 1.72-1.55 (m, 1H); MS (ES+), 287.3(M+1); (ES−): 285.3 (M−1).

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(tetrahydrofuran-3-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(81b)

Reaction ofN-(3-chloro-2-fluorobenzyl)-2-((tetrahydrofuran-3-yl)-amino)acetamide(81a) (110 mg, 0.38 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (93 mg, 0.42 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with CMA80 in CHCl₃ 0 to 60%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(tetrahydrofuran-3-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(81b) (136 mg, 0.28 mmol, 73% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.89 (t, J=5.6 Hz) and 8.49 (t, J=5.8 Hz) (2t, 1H), 8.25-8.09(m, 1H), 7.70 (s, 1H), 7.61-7.00 (m, 7H), 5.75-5.56 (m) and 5.40 (s)(2H), 4.95-4.71 (m, 1H), 4.47 (d, J=5.6 Hz) and 4.31 (d, J=5.5 Hz) (2d,2H), 4.25 (s) and 4.03-3.73 (m) (4H), 3.63-3.48 (m, 2H), 2.17-1.62 (m,2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.27, −121.73; MS (ES+) 488.5(M+1); 510.5 (M+Na); MS (ES−), 486.5 (M−1); [based on NMR, this compoundis a mixture of two rotamers 1:1 ratio].

Preparation of3-((2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)(phenyl)amino)propanamide(82e) Step-1: Preparation of tert-butyl2-((2-cyanoethyl)(phenyl)amino)acetate (82b)

Reaction of 3-(phenylamino)propanenitrile (82a) (1.0 g, 6.84 mmol) withtert-butyl 2-bromoacetate (1.11 mL, 7.52 mmol) using sodium hydride(0.274 g, 6.84 mmol) as a base according to the procedure reported instep-1 of Scheme 57 gave after workup and purification by flash columnchromatography [silica (40 g), eluting with EtOAc in hexane 0 to 50%]tert-butyl 2-((2-cyanoethyl)(phenyl)amino)acetate (82b) (148 mg, 0.57mmol, 8% yield) as a colorless oil; ¹H NMR (300 MHz, DMSO-d₆) δ7.24-7.11 (m, 2H), 6.76-6.51 (m, 3H), 4.09 (s, 2H), 3.70 (t, J=6.9 Hz,2H), 2.74 (t, J=6.8 Hz, 2H), 1.39 (s, 9H); MS (ES+): 283.5 (M+Na).

Step-2: Preparation of 2-((2-cyanoethyl)(phenyl)amino)acetic acid (82c)

Reaction of tert-butyl 2-((2-cyanoethyl)(phenyl)amino)acetate (82b) (141mg, 0.542 mmol) with TFA (0.42 mL, 5.42 mmol) according to the procedurereported in step-2 of Scheme 2 gave after workup2-((2-cyanoethyl)(phenyl)amino)acetic acid (82c) which was used as suchin the next step; MS (ES+): 205.3 (M+1); MS (ES−): 203.3 (M−1).

Step-3: Preparation ofN-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-2-((2-cyanoethyl)(phenyl)amino)-N-isopropylacetamide(82d)

Reaction of 2-((2-cyanoethyl)(phenyl)amino)acetic acid (82c) (110 mg,0.544 mmol) with N-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide(35b) (141 mg, 0.54 mmol) according to the procedure reported in step-3of Scheme 2 gave after workupN-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-2-((2-cyanoethyl)(phenyl)amino)-N-isopropylacetamide(82d) which was used as such in the next step; MS (ES−): 443.5 (M−1).

Step-4: Preparation of3-((2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)(phenyl)amino)propanamide(82e)

Reaction ofN-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-2-((2-cyanoethyl)(phenyl)amino)-N-isopropylacetamide(82d) (242 mg, 0.54 mmol) in ethanol (5 mL) using aq. NH₄OH (2.12 mL,54.4 mmol) and H₂O₂ (aq. 35%, 0.95 mL, 10.88 mmol) according to theprocedure reported in Scheme 65 gave after workup and purification byflash column chromatography [First column: silica gel (24 g), elutingwith MeOH in CHCl₃ 0-30%; Second column: Silica gel (12 g), eluting withMeOH in CHCl₃ 0-10%]3-((2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)(phenyl)amino)propanamide(82e) (53 mg, 0.11 mmol, 21% yield) as an off-white solid in the form ofmixture of two rotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 8.70 (t, J=5.8 Hz)and 8.28 (t, J=6.0 Hz) (2t, 1H), 7.56-7.31 (m, 3H), 7.30-7.15 (m, 1H),7.15-7.03 (m, 2H), 6.82 (bs, 1H), 6.70-6.49 (m, 3H), 4.67-4.52 and4.19-4.05 (m, 1H), 4.46-4.30 (m, 2H), 4.30 and 4.14 (2s, 2H), 4.01 and3.79 (2s, 2H), 3.57-3.44 (m, 2H), 2.41-2.31 (m, 2H), 1.18 (d, J=6.4 Hz)and 0.97 (d, J=6.8 Hz) (2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.30,−121.90; MS (ES+): 463.5 (M+1), 485.5 (M+Na); MS (ES−): 461.5 (M−1),497.5 (M+Cl).

Preparation of7-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-7H-pyrrolo[2,3-d]pyrimidine-4-carboxamide(83d) Step-1: Preparation of tert-butyl2-(4-cyano-7H-pyrrolo[2,3-d]pyrimidin-7-yl)acetate (83a)

To a degassed solution of tert-butyl2-(4-chloro-7H-pyrrolo[2,3-d]pyrimidin-7-yl)acetate (56b) (0.54 g, 2.02mmol) in DMA (10 mL) was added dicyanozinc (237 mg, 2.02 mmol),1,1′-binaphthyl-2-yldi-tert-butylphosphine (80 mg, 0.20 mmol),palladium(II)trifluoroacetate (34 mg, 0.10 mmol), Zn (66 mg, 1.01 mmol)and heated at 95° C. for 16 h. Mixture was cooled to room temperature,diluted with EtOAc (20 mL), filtered over Celite pad and washed withEtOAc (2×15 mL). The combined filtrate was washed with water (2×40 mL),brine, dried, filtered and concentrated in vacuum. The residue obtainedwas purified by flash column chromatography [silica gel (24 g), elutingwith EtOAc in hexanes 0 to 100%] to afford tert-butyl2-(4-cyano-7H-pyrrolo[2,3-d]pyrimidin-7-yl)acetate (83a) (80 mg, 0.31mmol, 15% yield) as white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 9.00 (s,1H), 8.01 (d, J=3.7 Hz, 1H), 6.90 (d, J=3.7 Hz, 1H), 5.14 (s, 2H), 1.41(s, 9H); MS (ES−): 257.3 (M−1).

Step-2: Preparation of tert-butyl2-(4-carbamoyl-7H-pyrrolo[2,3-d]pyrimidin-7-yl)acetate (83b)

Reaction of tert-butyl2-(4-cyano-7H-pyrrolo[2,3-d]pyrimidin-7-yl)acetate (83a) (350 mg, 1.36mmol) in ethanol (10 mL) using aq. NH₄OH (1.06 mL, 27.1 mmol) and H₂O₂(aq. 35%, 0.42 mL, 13.55 mmol) according to the procedure reported inScheme 65 gave after workup tert-butyl2-(4-carbamoyl-7H-pyrrolo[2,3-d]pyrimidin-7-yl)acetate (83b) (360 mg,1.30 mmol, 96% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 8.87(s, 1H), 8.33 (s, 1H), 7.88 (s, 1H), 7.76 (d, J=3.6 Hz, 1H), 7.07 (d,J=3.5 Hz, 1H), 5.09 (s, 2H), 1.41 (s, 9H); MS (ES+): 277.4 (M+1): MS(ES−): 275.3 (M−1).

Step-3: Preparation of2-(4-carbamoyl-7H-pyrrolo[2,3-d]pyrimidin-7-yl)acetic acid (83c)

Reaction of tert-butyl2-(4-carbamoyl-7H-pyrrolo[2,3-d]pyrimidin-7-yl)acetate (83b) (340 mg,1.23 mmol) with TFA (0.95 mL, 12.31 mmol) according to the procedurereported in step-2 of Scheme 2 gave after workup2-(4-carbamoyl-7H-pyrrolo[2,3-d]pyrimidin-7-yl)acetic acid (83c) whichwas used as such in the next step; MS (ES+): 221.3 (M+1); MS (ES−):219.2 (M−1).

Step-4: Preparation of7-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-7H-pyrrolo[2,3-d]pyrimidine-4-carboxamide(83d)

Reaction of N-(6-bromopyridin-2-yl)-2-(cyclopropylamino)acetamide (7c)(70 mg, 0.26 mmol) with2-(4-carbamoyl-7H-pyrrolo[2,3-d]pyrimidin-7-yl)acetic acid (83c) (57 mg,0.26 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column chromatography[silica gel (12 g), eluting with CMA80 in CHCl₃ 0 to 40%]7-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-7H-pyrrolo[2,3-d]pyrimidine-4-carboxamide(83d) (60 mg, 0.13 mmol, 49% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 10.94 (s, 1H), 8.86 (s, 1H), 8.31 (s, 1H), 8.01 (d, J=8.1 Hz,1H), 7.86 (s, 1H), 7.77-7.65 (m, 2H), 7.32 (dd, J=7.7, 0.7 Hz, 1H), 7.05(d, J=3.5 Hz, 1H), 5.50 (s, 2H), 4.17 (s, 2H), 3.14-3.02 (m, 1H),1.04-0.89 (m, 4H); MS (ES+): 472.5, 474.5 (M+1); MS (ES−); 470.4, 472.4(M−1).

Preparation of7-(2-((2-((6-bromopyrazin-2-yl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-7H-pyrrolo[2,3-d]pyrimidine-4-carboxamide(84a)

Reaction of N-(6-bromopyrazin-2-yl)-2-(cyclopropylamino)acetamide (49c)(70 mg, 0.26 mmol) with2-(4-carbamoyl-7H-pyrrolo[2,3-d]pyrimidin-7-yl)acetic acid (83c) (57 mg,0.26 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column chromatography[silica gel (12 g), eluting with CMA80 in CHCl₃ 0 to 40%]7-(2-((2-((6-bromopyrazin-2-yl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-7H-pyrrolo[2,3-d]pyrimidine-4-carboxamide(84a) (55 mg, 0.12 mmol, 45% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 11.28 (s, 1H), 9.24 (s, 1H), 8.86 (s, 1H), 8.54 (s, 1H), 8.31(s, 1H), 7.85 (s, 1H), 7.72 (d, J=3.5 Hz, 1H), 7.05 (d, J=3.5 Hz, 1H),5.51 (s, 2H), 4.22 (s, 2H), 3.15-3.05 (m, 1H), 1.06-0.92 (m, 4H); MS(ES+): 473.4 and 475.4 (M+1); MS (ES−): 471.3 and 473.3 (M−1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cycloheptyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(85b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-(cycloheptylamino)acetamide (85a)

Reaction of 2-bromo-N-(3-chloro-2-fluorobenzyl)acetamide (69b) (313 mg,1.12 mmol) with cycloheptanamine (0.17 mL, 1.34 mmol) according to theprocedure reported in step-2 of Scheme 35 gave after workupN-(3-chloro-2-fluorobenzyl)-2-(cycloheptylamino)acetamide (85a) as ayellow oil which was used as such without further purification; MS(ES+): 313.4 (M+1); MS (ES−): 311.4 (M−1), 347.4 (M+Cl).

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cycloheptyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(85b)

Reaction of N-(3-chloro-2-fluorobenzyl)-2-(cycloheptylamino)acetamide(85a) (347 mg, 1.12 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (365 mg, 1.66 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (40 g), eluting with MeOH in CHCl₃ 0 to 10%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cycloheptyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(85b) (136 mg, 0.27 mmol, 24% yield) as an off-white solid as a mixtureof two rotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 8.85 (t, J=5.8 Hz) & 8.37(t, J=5.9 Hz) (2t, 1H), 8.23-8.13 (m, 1H), 7.70 (s, 1H), 7.65-7.35 (m,5H), 7.32-6.96 (m, 2H), 5.59 & 5.46 (s, 2H), 4.46 (d, J=5.6 Hz) & 4.31(d, J=5.7 Hz) (2d, 2H), 4.27-4.21 & 3.98-3.87 (m, 1H), 4.19 & 3.82 (2s,2H), 1.69-1.40 (m, 11H), 1.36-1.23 (m, 1H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.10, −121.72; MS (ES+): 514.8 and 516.7 (M+1), 536.7 and 538.6(M+Na); MS (ES−): 512.3, 514.6 (M−1), 548.5 (M+Cl).

Preparation of2-(4-chloro-1H-pyrrolo[2,3-b]pyridin-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(86d) Step-1: Preparation of tert-butyl2-(4-chloro-1H-pyrrolo[2,3-b]pyridin-1-yl)acetate (86b)

Reaction of 4-chloro-1H-pyrrolo[2,3-b]pyridine (86a) (2.0 g, 13.11 mmol)with tert-butyl 2-bromoacetate (2.32 mL, 15.73 mmol) according to theprocedure reported in step-1 of Scheme 56 gave after workup andpurification by flash column chromatography [silica (40 g), eluting withEtOAc in hexane 0 to 50%] tert-butyl2-(4-chloro-1H-pyrrolo[2,3-b]pyridin-1-yl)acetate (86b) (3 g, 11.25mmol, 86% yield) as a colorless oil; ¹H NMR (300 MHz, DMSO-d₆) δ 8.21(d, J=5.2 Hz, 1H), 7.66 (d, J=3.6 Hz, 1H), 7.26 (d, J=5.2 Hz, 1H), 6.56(d, J=3.6 Hz, 1H), 5.05 (s, 2H), 1.40 (s, 9H).

Step-2: Preparation of 2-(4-chloro-1H-pyrrolo[2,3-b]pyridin-1-yl)aceticacid (86c)

Reaction of tert-butyl 2-(4-chloro-1H-pyrrolo[2,3-b]pyridin-1-yl)acetate(86b) (1.5 g, 5.62 mmol) with TFA (4.33 mL, 56.2 mmol) according to theprocedure reported in step-2 of Scheme 2 gave after workup2-(4-chloro-1H-pyrrolo[2,3-b]pyridin-1-yl)acetic acid (86c) (940 mg,4.46 mmol, 79% yield) as light orange solid; ¹H NMR (300 MHz, DMSO-d₆) δ13.08 (s, 1H), 8.20 (d, J=5.2 Hz, 1H), 7.67 (d, J=3.6 Hz, 1H), 7.26 (d,J=5.2 Hz, 1H), 6.56 (d, J=3.6 Hz, 1H), 5.06 (s, 2H); MS (ES+): 211.2(M+1); (ES−) 209.1 (M−1).

Step-3: Preparation of2-(4-chloro-1H-pyrrolo[2,3-b]pyridin-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(86d)

Reaction of 2-(4-chloro-1H-pyrrolo[2,3-b]pyridin-1-yl)acetic acid (86c)(330 mg, 1.57 mmol) withN-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide (10b) (402 mg,1.57 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column [silica gel (24 g),eluting with MeOH-EtOAc (1:9) in hexanes 0 to 70%]2-(4-chloro-1H-pyrrolo[2,3-b]pyridin-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(86d) (580 mg, 1.29 mmol, 82% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.45 (t, J=5.8 Hz, 1H), 8.18 (d, J=5.2 Hz, 1H), 7.61 (d,J=3.6 Hz, 1H), 7.47 (td, J=7.6, 1.8 Hz, 1H), 7.29-7.18 (m, 2H),7.18-7.10 (m, 1H), 6.56 (d, J=3.5 Hz, 1H), 5.44 (s, 2H), 4.33 (d, J=5.7Hz, 2H), 3.97 (s, 2H), 3.09-2.98 (m, 1H), 1.05-0.87 (m, 4H); ¹⁹F NMR(282 MHz, DMSO-d₆) δ −121.61; MS (ES−): 447.3 and 449.5 (M−1), 483.4 and485.4 (M+Cl).

Preparation of2-(4-acetamido-1H-pyrrolo[2,3-b]pyridin-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(87a)

To a degassed solution of2-(4-chloro-1H-pyrrolo[2,3-b]pyridin-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(86d) (300 mg, 0.67 mmol) in dioxane (10 mL) was added cesium carbonate(326 mg, 1.0 mmol), acetamide (79 mg, 1.34 mmol),dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine (32 mg, 0.067mmol), Pd₂(dba)₃ (31 mg, 0.033 mmol) and heated at 80° C. for 16 h. Themixture was cooled to room temperature, diluted with EtOAc (5 mL),filtered over Celite pad and pad was washed with EtOAc (2×5 mL). Thefiltrate was washed with water (2×30 mL), brine, dried, filtered andconcentrated in vacuum. The residue was purified by flash columnchromatography [silica gel (12 g), eluting with CMA80 in CHCl₃ 0 to 40%]to afford2-(4-acetamido-1H-pyrrolo[2,3-b]pyridin-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(87a) (105 mg, 0.22 mmol, 33% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 10.05 (s, 1H), 8.44 (t, J=5.9 Hz, 1H), 8.06 (d, J=5.4 Hz,1H), 7.83 (d, J=5.4 Hz, 1H), 7.51-7.41 (m, 1H), 7.35 (d, J=3.6 Hz, 1H),7.27-7.07 (m, 2H), 6.82 (d, J=3.6 Hz, 1H), 5.37 (s, 2H), 4.33 (d, J=5.8Hz, 2H), 3.97 (s, 2H), 3.09-2.97 (m, 1H), 2.20 (s, 3H), 1.03-0.84 (m,4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.62; MS (ES+) 472.5 (M+1); MS(ES−): 470.5 (M−1), 506.5 (M+Cl).

Preparation of tert-butyl4-(2-(3-carbamoyl-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)acetamido)piperidine-1-carboxylate(88b) Step-1: Preparation of tert-butyl4-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)piperidine-1-carboxylate(88a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (500 mg,5.3 mmol) with tert-butyl 4-aminopiperidine-1-carboxylate (1.06 g, 5.3mmol) according to the procedure reported in step-2 of Scheme 35 gaveafter workup and purification by flash column chromatography [silica (12g), eluting with EtOAc/MeOH (9:1) in hexane 0 to 60%] tert-butyl4-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)piperidine-1-carboxylate(88a) (762 mg, 1.91 mmol, 90%) as a clear oil. ¹H NMR (300 MHz, DMSO-d₆)δ 8.38 (t, J=6.1 Hz, 1H), 7.53-7.40 (m, 1H), 7.34-7.23 (m, 1H),7.23-7.14 (m, 1H), 4.36 (d, J=6.0 Hz, 2H), 3.79 (d, J=13.1 Hz, 2H), 3.16(s, 2H), 2.87-2.63 (m, 2H), 2.48-2.40 (m, 1H), 2.27 (s, 1H), 1.79-1.64(m, 2H), 1.38 (s, 9H), 1.20-1.01 (m, 2H); MS (ES+): 400.5 (M+1); MS(ES−): 398.4 (M−1).

Step-2: Preparation of tert-butyl4-(2-(3-carbamoyl-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)acetamido)piperidine-1-carboxylate(88b)

Reaction of tert-butyl4-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)piperidine-1-carboxylate(88a) (660 mg, 1.65 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (398 mg, 1.82 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with CMA80 in CHCl₃ 0 to 60%]tert-butyl4-(2-(3-carbamoyl-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)acetamido)piperidine-1-carboxylate(88b) (442 mg, 0.74 mmol, 45% yield) as a white solid; NMR (300 MHz,DMSO-d₆) δ 8.78 (t, J=5.7 Hz) and 8.36 (t, J=5.8 Hz) (2t, 1H), 8.18 (m,1H), 7.71 (m, 1H), 7.60-7.06 (m, 7H), 5.67 and 5.48 (2s, 2H), 4.46 (d,J=3.7 Hz) and 4.31 (d, J=4.9 Hz) (2d, 2H), 4.21 and 3.86 (2s, 2H),4.37-3.90 (m, 3H), 2.77 (m, 2H), 1.40 (m, 13H); ¹⁹F NMR (282 MHz, DMSO)δ −121.12, −121.67; MS (ES+): 623.6 & 625.7 (M+Na); [based on NMR, thiscompound is a mixture of rotamers 2:1 ratio].

Preparation of(R)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(piperidin-3-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(89c) Step-1: Preparation of (R)-tert-butyl3-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)piperidine-1-carboxylate(89a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (500 mg,5.3 mmol) with (R)-tert-butyl 3-aminopiperidine-1-carboxylate (1.06 g,5.3 mmol) according to the procedure reported in step-2 of Scheme 35gave after workup and purification by flash column chromatography[silica (12 g), eluting with EtOAc/MeOH (9:1) in hexane 0 to 60%](R)-tert-butyl3-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)piperidine-1-carboxylate(89a) (850 mg, 2.13 mmol, 100%) as a yellow oil; MS (ES+): 400.5 (M+1);MS (ES−): 398.4 (M−1).

Step-2: Preparation of (R)-tert-butyl3-(2-(3-carbamoyl-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)acetamido)piperidine-1-carboxylate(89b)

Reaction of (R)-tert-butyl3-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)piperidine-1-carboxylate(89a) (710 mg, 1.78 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (428 mg, 1.95 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with CMA80 in CHCl₃ 0 to 60%](R)-tert-butyl3-(2-(3-carbamoyl-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)acetamido)piperidine-1-carboxylate(89b) (520 mg, 0.87 mmol, 49% yield) as a white solid. MS (ES+): 602.6(M+1).

Step-3: Preparation of(R)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(piperidin-3-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(89c)

Reaction of (R)-tert-butyl3-(2-(3-carbamoyl-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)acetamido)piperidine-1-carboxylate(89b) (495 mg, 0.82 mmol) with TFA (0.32 mL, 4.12 mmol) according to theprocedure reported in step-2 of Scheme 2 gave after workup andpurification by flash column chromatography [silica (12 g), eluting withCMA80 in CHCl₃ 0 to 60%](R)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(piperidin-3-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(89c) (300 mg, 0.6 mmol, 73% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.82 (t, J=5.6 Hz) and 8.37 (t, J=5.9H) (2t, 1H), 8.18 (d,J=8.1 Hz, 1H), 7.78-7.64 (m, 1H), 7.63-7.03 (m, 7H), 5.75-5.51 (m) and5.45 (s) (2H), 4.52-4.38 (m, 1H), 4.31 (d, J=5.7 Hz) and 4.22 (d, J=4.6Hz) (2d, 2H), 4.17-4.04 and 3.85-3.75 (2m, 1H), 3.89 and 3.17 (2s, 2H),3.12-2.65 (m, 2H), 2.45-2.18 (m, 2H), 1.96-1.25 (m, 4H); ¹⁹F NMR (282MHz, DMSO-d₆) δ −73.45 (TFA peak), −121.17, −121.70; MS (ES+) 501.5(M+1); 499.5 (M−1); [based on NMR, this compound is a mixture ofrotamers 2:1 ratio].

Preparation of2-(3-acetyl-5-bromo-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(90d) Step-1: Preparation of tert-butyl2-(3-acetyl-5-bromo-1H-indol-1-yl)acetate (90b)

Reaction of 1-(5-bromo-1H-indol-3-yl)ethanone (90a) (prepared accordingto the procedure reported By Denis, Jean-Noeel et al in PCT Int. Appl.,WO 2013/014102, 8.24 g, 34.6 mmol) with tert-butyl 2-bromoacetate (6.14mL, 41.5 mmol) according to the procedure reported in step-1 of Scheme56 gave after workup tert-butyl2-(3-acetyl-5-bromo-1H-indol-1-yl)acetate (90b) (11.26 g, 32.0 mmol, 92%yield) as an off-white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 8.38 (s, 1H),8.35-8.29 (m, 1H), 7.54-7.36 (m, 2H), 5.14 (s, 2H), 2.44 (s, 3H), 1.43(s, 9H); MS (ES+): 352.2, 354.3 (M+2), 374.4, 376.3 (M+Na); (ES−):350.3, 352.3 (M−2), 386.3, 388.3 (M+Cl).

Step-2: Preparation of 2-(3-acetyl-5-bromo-1H-indol-1-yl)acetic acid(90c)

Reaction of tert-butyl 2-(3-acetyl-5-bromo-1H-indol-1-yl)acetate (90b)(11.15 g, 31.7 mmol) with TFA (48.8 mL, 633 mmol) according to theprocedure reported in step-2 of Scheme 2 gave after workup2-(3-acetyl-5-bromo-1H-indol-1-yl)acetic acid (90c) (11.38 g, 38.4 mmol,88% yield) as a pink solid in the form of TFA adduct; ¹H NMR (300 MHz,DMSO-d₆) δ 13.33 (bs, 1H, D₂O exchangeable), 8.40 (s, 1H), 8.32 (d,J=2.0 Hz, 1H), 7.54 (d, J=8.8, 1H), 7.40 (dd, J=8.7, 2.0 Hz, 1H), 5.15(s, 2H), 2.44 (s, 3H); MS (ES+): 296.2, 298.2 (M+2); (ES−) 294.2, 296.2(M−2).

Step-3: Preparation of2-(3-acetyl-5-bromo-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(90d)

Reaction of 2-(3-acetyl-5-bromo-1H-indol-1-yl)acetic acid (90c) (1.6 g,5.4 mmol) with N-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide(19c) (1.4 g, 5.4 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup and purification by flash column [silica gel(40 g), eluting with MeOH in CHCl₃ 0-100%]2-(3-acetyl-5-bromo-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(90d) (1.67 g, 3.11 mmol, 58% yield) as a pale yellow solid as ofmixture of two rotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 8.83 (t, J=5.7 Hz,1H), 8.36-8.28 (m, 2H, another triplet of amide proton of one of the tworotamers were overlapped in this region), 7.56-7.29 (m, 4H), 7.22 (td,J=7.9, 1.1 Hz) & 6.99 (td, J=7.9, 1.1 Hz) (2td, 1H), 5.37 & 5.18 (2s,2H), 4.65-4.51 & 4.27-4.18 (2m, 1H), 4.47 (d, J=5.6 Hz) & 4.33 (d, J=5.8Hz) (2d, 2H), 4.17 & 3.84 (2s, 2H), 2.44 & 2.42 (2s, 3H), 1.25 (d, J=6.4Hz) & 0.99 (d, J=6.8 Hz) (2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.19,−121.76; MS (ES+): 536.49 and 538.49 (M+1), 558.5 and 560.5 (M+Na);(ES−): 534.36 and 536.41 (M−1), 570.4 and 572.4 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(piperidin-4-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(91a)

Reaction of tert-butyl4-(2-(3-carbamoyl-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)acetamido)piperidine-1-carboxylate(88b) (500 mg, 0.92 mmol) with TFA (0.35 mL, 4.58 mmol) according to theprocedure reported in step-2 of Scheme 2 gave after workup andpurification by flash column chromatography [silica (12 g), eluting withCMA80 in CHCl₃ 0 to 60%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(piperidin-4-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(91a) (386 mg, 0.77 mmol, 84% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.89 (t, J=5.6 Hz) and 8.42 (t, J=5.9 Hz) (2t, 1H), 8.23-8.12(m, 1H), 7.77-7.64 (m, 1H), 7.64-7.04 (m, 7H), 5.65 and 5.44 (s, 2H),4.47 (d, J=5.4 Hz) and 4.32 (d, J=5.7 Hz) (2d, 2H), 4.21 and 3.84 (2s,2H), 4.32-4.30 and 4.12-3.95 (2m, 1H), 3.22-3.01 (m, 2H), 2.85-2.69 and2.69-2.56 (2m, 2H), 1.94-1.40 (m, 4H); ¹⁹F NMR (282 MHz, DMSO) δ −73.53(TFA peak), −121.18, −121.66; MS (ES+): 501.6 (M+1); 499.5 (M−1); [basedon NMR, this compound is a mixture of rotamers 3:2 ratio].

Preparation of2-(3-acetyl-5-(phenylethynyl)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(92a)

A solid mixture of2-(3-acetyl-5-bromo-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(90d) (113 mg, 0.21 mmol), Cs₂CO₃ (69 mg, 0.21 mmol),dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine (X-PHOS, 20mg, 0.04 mmol), Pd₂(dba)₃ (19 mg, 0.02 mmol) was purged with positiveflow of nitrogen for 10 min, then added phenylacetylene (0.023 mL, 0.21mmol) and anhydrous toluene (10 mL) under a positive flow of nitrogen.The reaction flask was heated at 90° C. for 8 h. The reaction mixturewas diluted with EtOAc (50 mL), filtered through a Celite pad,subsequently pad was rinsed with EtOAc (3×20 mL). The filtrate waswashed with brine, dried, filtered and evaporated to dryness. Theresidue was purified by flash column chromatography [silica gel (24 g),eluting with MeOH in CHCl₃ 0 to 20%] to afford2-(3-acetyl-5-(phenylethynyl)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(92a) (63 mg, 54% yield) as a brown solid as a mixture of two rotamers;¹H NMR (300 MHz, DMSO-d₆) δ 8.84 (t, J=5.7 Hz) and 8.43-8.26 (m) (3H),7.63-7.34 (m, 9H), 7.30-6.96 (m, 1H), 5.39 & 5.21 (2s, 2H), 4.67-4.53 &4.32-4.19 (2m, 1H), 4.48 (d, J=5.9 Hz) & 4.34 (d, J=5.8 Hz) (2d, 2H),4.19 & 3.86 (2s, 2H), 2.46 & 2.44 (2s, 3H), 1.26 (d, J=6.4 Hz) & 1.01(d, J=6.8 Hz) (2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.18, −121.77;MS (ES+): 558.7 & 560.6 (M+1); (ES−): 556.6 & 558.6 (M−1).

Preparation of (5)-tert-butyl3-(2-(3-carbamoyl-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)acetamido)pyrrolidine-1-carboxylate(93b) Step-1: Preparation of (S)-tert-butyl3-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)pyrrolidine-1-carboxylate(93a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (350 mg,1.48 mmol) with (S)-tert-butyl 3-aminopyrrolidine-1-carboxylate (690 mg,3.71 mmol) according to the procedure reported in step-2 of Scheme 35gave after workup and purification by flash column chromatography[silica (12 g), eluting with EtOAc/MeOH (9:1) in hexane 0 to 60%](5)-tert-butyl3-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)pyrrolidine-1-carboxylate(93a) (500 mg, 1.3 mmol, 87%) as a yellow oil; MS (ES+): 386.5 (M+1).

Step-2: Preparation of (S)-tert-butyl3-(2-(3-carbamoyl-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)acetamido)pyrrolidine-1-carboxylate(93b)

Reaction of (5)-tert-butyl3-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)pyrrolidine-1-carboxylate(93a) (300 mg, 0.78 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (187 mg, 0.86 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with CMA80 in CHCl₃ 0 to 60%](5)-tert-butyl3-(2-(3-carbamoyl-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)acetamido)pyrrolidine-1-carboxylate(93b) (352 mg, 0.6 mmol, 77% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.83 (t, J=5.6 Hz) and 8.44 (t, J=5.0 Hz) (2t, 1H), 8.22-8.13(m, 1H), 7.77-7.65 (m, 1H), 7.64-7.01 (m, 7H), 5.70 and 5.42 (2s, 2H),4.84-4.63 (m, 1H), 4.47 (d, J=5.1 Hz) and 4.31 (d, J=5.7 Hz) (2d, 2H),4.26 and 3.91 (2s, 2H), 3.46-2.95 (m, 2H), 2.19-1.80 (m, 2H), 1.41 and1.37 (2s, 9H), 0.89-0.77 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.24,−121.68; MS (ES+): 587.6 (M+1); MS (ES−): 585.6 (M−1); [based on NMR,this compound is a mixture of rotamers]

Preparation of(S)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(94b) Step-1: Preparation of(S)—N-(3-chloro-2-fluorobenzyl)-2-((1-hydroxypropan-2-yl)amino)acetamide(94a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (350 mg,1.48 mmol) with (S)-2-aminopropan-1-ol (278 mg, 3.71 mmol) according tothe procedure reported in step-2 of Scheme 35 gave after workup andpurification by flash column chromatography [silica (12 g), eluting withEtOAc/MeOH (9:1) in hexane 0 to 60%](S)—N-(3-chloro-2-fluorobenzyl)-2-((1-hydroxypropan-2-yl)amino)acetamide(94a) (200 mg, 0.73 mmol, 49%) as a yellow oil; MS (ES+): 275.4, 277.4(M+1, M+3).

Step-2: Preparation of(S)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(94b)

Reaction of(S)—N-(3-chloro-2-fluorobenzyl)-2-((1-hydroxypropan-2-yl)amino)acetamide(94a) (200 mg, 0.73 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (176 mg, 0.8 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with CMA80 in CHCl₃ 0 to 60%](S)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxo ethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide (94b) (210 mg,0.44 mmol, 61% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ8.90-8.46 (m, 1H), 8.25-8.12 (m, 1H), 7.72 (s, 1H), 7.60-6.89 (m, 7H),5.83-5.31 (m, 3H), 4.86-4.11 (m, 4H), 4.00-3.72 (m, 1H), 3.55-3.39 (m,1H), 3.32-3.13 (m, 1H), 1.17-0.88 (m, 3H); ¹⁹F NMR (282 MHz, DMSO) δ−121.26, −121.65; MS (ES+): 476.5 (M+1); (ES−): 474.5 (M−1); [based onNMR, this compound is a mixture of rotamers]

Preparation of(R)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(4-hydroxybutan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(95b) Step-1: Preparation of(R)—N-(3-chloro-2-fluorobenzyl)-2-((4-hydroxybutan-2-yl)amino)acetamide(95a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (500 mg,2.12 mmol) with (R)-3-aminobutan-1-ol (378 mg, 4.24 mmol) according tothe procedure reported in step-2 of Scheme 35 gave after workup andpurification by flash column chromatography [silica (12 g), eluting withEtOAc/MeOH (9:1) in hexane 0 to 60%](R)—N-(3-chloro-2-fluorobenzyl)-2-((4-hydroxybutan-2-yl)amino)acetamide(95a) (150 mg, 0.52 mmol, 25%) as a yellow oil; MS (ES+): 289.4 (M+1);MS (ES−): 287.3 (M−1).

Step-2: Preparation of(R)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(4-hydroxybutan-2-yl)amino)-2-oxo ethyl)-1H-indazole-3-carboxamide (95b)

Reaction of(R)—N-(3-chloro-2-fluorobenzyl)-2-((4-hydroxybutan-2-yl)amino)acetamide(95a) (150 mg, 0.52 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (125 mg, 0.57 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with CMA80 in CHCl₃ 0 to 60%](R)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(4-hydroxybutan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(95b) (43 mg, 0.088 mmol, 17% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.90-8.46 (m, 1H), 8.25-8.12 (m, 1H), 7.72 (s, 1H), 7.60-6.89(m, 7H), 5.83-5.31 and 4.86-4.11 and 4.00-3.72 (3m, 8H), 3.55-3.39 and3.32-3.13 (2m, 2H), 1.17-0.88 (m, 3H); ¹⁹F NMR (282 MHz, DMSO) δ−121.26, −121.77; MS (ES+): 490.5 (M+1); (ES−): 488.5 (M−1); [based onNMR, this compound is a mixture of rotamers 1:1 ratio].

Preparation of2-(3-acetyl-5-bromo-1H-indol-1-yl)-N-(2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)-N-isopropylacetamide(96a)

Reaction of N-(6-bromopyridin-2-yl)-2-(isopropylamino)acetamide (28b)(1.1 g, 4.05 mmol) with 2-(3-acetyl-5-bromo-1H-indol-1-yl)acetic acid(90c) (1.2 g, 4.05 mmol) according to the procedure reported in step-3of Scheme 2 gave after workup2-(3-acetyl-5-bromo-1H-indol-1-yl)-N-(2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)-N-isopropylacetamide(96a) (1.5 g, 2.73 mmol, 67% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) (as a mixture of rotamers) δ 11.20 and 10.81 (2s, 1H),8.36-8.28 (m, 2H), 8.17 and 8.01 (2d, J=8.1 Hz, 1H), 7.81 and 7.70 (2t,J=8.0 Hz, 1H), 7.48-7.27 (m, 3H), 5.41 and 5.20 (2s, 2H), 4.69-4.55 and4.32-4.20 (2m, 1H), 4.42 and 4.04 (2s, 2H), 2.44 and 2.43 (2s, 3H), 1.26and 1.03 (2d, J=6.4 Hz, 6H); MS (ES+): 551.4, 553.4 (M+1); MS (ES−):583.4, 585.4 (M+Cl).

Preparation of2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(97c) Step-1: Preparation of tert-butyl2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)acetate (97a)

To a degassed DMF (12 mL) in a sealed reactor were added tert-butyl2-(3-acetyl-5-bromo-1H-indol-1-yl)acetate (90b) (1.05 g, 2.98 mmol),cesium carbonate (1.94 g, 5.96 mmol), pyrimidin-5-amine (340 mg, 3.58mmol), Pd₂(dba)₃ (273 mg, 0.3 mmol),(9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (Xanthphos,172 mg, 0.3 mmol) and heated with stirring at 100° C. for 16 h. Themixture was cooled to room temperature, diluted with EtOAc (30 mL) andfiltered over Celite pad. The pad was washed with EtOAc (2×15 mL) andcombined filtrate was concentrated to give a crude residue which waspurified by flash column chromatography [silica gel (40 g), eluting withCMA80 in CHCl₃ 0 to 20%] to afford tert-butyl2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)acetate (97a) (0.34 g,0.93 mmol, 31% yield) as light yellow solid; MS (ES+): 367.5 (M+1), MS(ES−): 401.4 (M+Cl).

Step-2: Preparation of2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)acetic acid (97b)

Reaction of tert-butyl2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)acetate (97a) (340 mg,0.93 mmol) with TFA (1.43 mL, 18.56 mmol) according to the procedurereported in step-2 of Scheme 2 gave after workup2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)acetic acid (97b) (250mg, 0.81 mmol, 87% yield) as light orange solid. ¹H NMR showed productas mixture of rotamers and data is corresponding to the major rotamer;¹H NMR (300 MHz, DMSO-d₆) δ 13.7-13.1 (bs, 1H, D₂O exchangeable),8.67-8.51 (m, 2H), 8.48 (s, 2H), 8.31 (s, 1H), 8.01 (d, J=2.2 Hz, 1H),7.48 (d, J=8.8 Hz, 1H), 7.18-7.07 (m, 1H), 5.11 (s, 2H), 2.41 (s, 3H);MS (ES+) 311.4 (M+1), MS (ES−) 309.3 (M−1).

Step-3: Preparation of2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(97c)

Reaction of 2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)aceticacid (97b) (80 mg, 0.26 mmol) withN-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide (19c) (67 mg,0.26 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column [silica gel (12 g),eluting with CMA-80 in CHCl₃ 0-100%]2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(97c) (68 mg, 0.12 mmol, 48% yield) as an off-white solid; ¹H NMR (300MHz, DMSO-d₆) (as a mixture of two rotamers) δ 8.83 and 8.35 (2t, J=5.8Hz, 1H), 8.57 and 8.56 (2s, 1H), 8.49 (s, 1H), 8.47 (s, 2H), 8.25 and8.20 (2s, 1H), 8.00 (d, J=2.2 Hz, 1H), 7.57-7.34 (m, 3H), 7.25-6.96 (m,2H), 5.34 and 5.15 (2s, 2H), 4.69-4.51 and 4.28-4.21 (2m, 1H), 4.47 and4.34 (2d, J=5.6 Hz, 2H), 4.18 and 3.85 (2s, 2H), 2.41 and 2.40 (2s, 3H),1.25 and 1.00 (2d, J=6.8 Hz, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) (as amixture of two rotamers) δ −121.18 and −121.77; MS (ES+): 551.6 (M+1),MS (ES−): 549.5 (M−1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-cyclopropylethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(98b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-((l-cyclopropylethyl)amino)acetamide (98a)

Reaction of 2-bromo-N-(3-chloro-2-fluorobenzyl)acetamide (69b) (307 mg,1.09 mmol) with 1-cyclopropylethanamine (93 mg, 1.09 mmol) according tothe procedure reported in step-2 of Scheme 35 gave after workupN-(3-chloro-2-fluorobenzyl)-2-((1-cyclopropylethyl)amino)acetamide (98a)as a yellow oil which was used as such without further purification; MS(ES+): 285.4 (M+1); MS (ES−): 283.3 (M−1).

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-cyclopropylethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(98b)

Reaction ofN-(3-chloro-2-fluorobenzyl)-2-((1-cyclopropylethyl)amino)acetamide (98a)(312 mg, 1.1 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e)(288 mg, 1.32 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup and purification by flash columnchromatography [silica (40 g), eluting with MeOH in CHCl₃ 0 to 10%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-cyclopropylethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(98b) (115 mg, 0.24 mmol, 22% yield) as a pale yellow solid as a mixtureof two rotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 8.82 (t, J=5.7 Hz) and 8.30(t, J=5.9 Hz) (2t, 1H), 8.22-8.13 (m, 1H), 7.74 and 7.70 (2s, 1H),7.61-7.33 (m, 5H), 7.30-7.00 (m, 2H), 5.76-5.35 (m, 2H), 4.54-4.21 (m)and 3.96 (s) (4H), 3.80-3.46 (m, 1H), 1.27 (d, J=6.4 Hz) and 1.02 (d,J=6.8 Hz) (2d, 3H), 0.93-0.76 (m) and 0.64-0.37 (m) and 0.31-0.14 (m)and 0.13-0.02 (m) (5H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.19, −121.75;MS (ES+): 486.5 (M+1), 508.5 (M+Na); (ES−) 484.5 (M−1), 520.5 (M+Cl).

Preparation of2-(3-acetyl-5-((trimethylsilyl)ethynyl)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(99a)

Reaction of2-(3-acetyl-5-bromo-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(90d) (504 mg, 0.94 mmol) with ethynyltrimethylsilane (0.13 mL, 0.94mmol) according to the procedure reported in scheme 92 gave after workupand purification by flash column chromatography [silica gel (40 g),eluting with MeOH in CHCl₃ 0 to 100%; second column: silica gel (12 g),eluting with MeOH/EtOAc (9:1) in hexanes 0 to 100%]2-(3-acetyl-5-((trimethylsily)ethynyl)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(99a) (21 mg, 0.038 mmol, 4% yield) as a yellow solid as a mixture oftwo rotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 8.84 (t, J=5.8 Hz) and8.42-8.22 (m) (3H), 7.62-6.96 (m, 5H), 5.37 and 5.19 (2s, 2H), 4.65-4.52and 4.26-4.21 (2m, 1H), 4.47 (d, J=5.6 Hz) and 4.32 (d, J=5.7 Hz) (2d,2H), 4.17 and 3.84 (2s, 2H), 2.44 and 2.42 (2s, 3H), 1.25 (d, J=6.4 Hz)and 0.99 (d, J=6.8 Hz) (2d, 6H), 0.40-0.08 (m, 9H); ¹⁹F NMR (282 MHz,DMSO-d₆) δ −121.20, −121.77 (d, J=4.0 Hz); MS (ES+): 554.6 & 556.6(M+1), 576.6 & 578.7 (M+Na); MS (ES−): 588.5 & 590.6 (M+Cl).

Preparation of2-(3-acetyl-5-(1-methyl-1H-pyrazol-3-yl)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(100a)

To a degassed solution of2-(3-acetyl-5-bromo-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(90d) (150 mg, 0.28 mmol),1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (70mg, 0.335 mmol) in dioxane (4 mL) was added a solution of K₂CO₃ (1.12mL, 0.56 mmol) in water (1 mL) followed by tetrakistriphenylphosphinePalladium(0) (32 mg, 0.028 mmol) and heated at 80° C. for 4h. Themixture was cooled to room temperature and diluted with EtOAc (50 mL)and water (60 mL). The organic layer was separated washed with brine,dried, filtered and concentrated in vacuum. The residue obtained waspurified by flash column chromatography [silica gel (12 g), eluting withCMA80 in CHCl₃ 0 to 30%] to afford2-(3-acetyl-5-(1-methyl-1H-pyrazol-3-yl)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(100a) (85 mg, 0.16 mmol, 57% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) (a mixture of two rotamers in 2:1 ratio) δ 8.83 and 8.35 (2t,J=6.0 Hz, 1H), 8.31-8.27 (m, 1H), 8.24 and 8.19 (2s, 1H), 8.10 (s, 1H),7.83-7.76 (m, 1H), 7.55-7.35 (m, 4H), 7.26-7.17 and 7.05-6.96 (2m, 1H),5.34 and 5.16 (2s, 2H), 4.65-4.52 and 4.30-4.21 (2m, 1H), 4.48 and 4.34(2d, J=5.6 Hz, 2H), 4.18 and 3.85 (2s, 2H), 3.88 and 3.87 (2s, 3H), 2.44and 2.42 (2s, 3H), 1.25 and 1.00 (2d, J=6.4 Hz, 6H); NMR (282 MHz,DMSO-d₆) (a mixture of two rotamers) δ −121.19 and −121.79; MS (ES+):538.6 (M+1), 560.6 (M+Na); MS (ES): 536.6 (M−1).

Preparation of2-(3-acetyl-5-(2-(dimethylamino)pyrimidin-5-yl)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(101a)

Reaction of2-(3-acetyl-5-bromo-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(90d) (150 mg, 0.28 mmol) with (2-(dimethylamino)pyrimidin-5-yl)boronicacid (56 mg, 0.34 mmol) according the procedure reported in Scheme 100gave after workup and purification by flash column chromatography[silica gel (12 g), eluting with CMA80 in CHCl₃ 0 to 30%]2-(3-acetyl-5-(2-(dimethylamino)pyrimidin-5-yl)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(101a) (26 mg, 0.045 mmol, 16% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) (mixture of rotamers) 8.83 and 8.35 (2t, J=5.2 Hz, 1H), 8.65and 8.646 (2s, 2H), 8.31 and 8.26 (2s, 1H), 7.60-7.47 (m, 2H), 7.47-7.36(m, 2H), 7.28-7.16 and 7.07-6.95 (2m, 2H), 5.38 and 5.20 (2s, 2H),4.65-4.53 and 4.29-4.22 (2m, 1H), 4.48 and 4.33 (2d, J=5.6 Hz, 2H), 4.19and 3.85 (2s, 2H), 3.25-3.10 (m, 6H), 2.45 and 2.44 (2s, 3H), 1.26 and1.00 (d, J=6.8 Hz, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) (a mixture of tworotamers) δ −121.18 and −121.78; MS (ES+): 579.7 (M+1), 601.7 (M+Na), MS(ES−): 577.6 (M−1).

Preparation of1-(2-((3-amino-3-oxopropyl)(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(102b) Step-1: Preparation of3-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)propanamide(102a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (350 mg,1.48 mmol) with 3-aminopropanamide hydrochloride (462 mg, 3.71 mmol)according to the procedure reported in step-2 of Scheme 35 gave afterworkup and purification by flash column chromatography [silica (12 g),eluting with EtOAc/MeOH (9:1) in hexane 0 to 60%]3-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)propanamide(102a) (168 mg, 0.77 mmol, 52%) as a yellow oil; MS (ES+): 288.4 (M+1),310.3 (M+Na); (ES−): 286.3 (M−1).

Step-2: Preparation of1-(2-((3-amino-3-oxopropyl)(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(102b)

Reaction of3-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)propanamide(102a) (168 mg, 0.77 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (200 mg, 0.7 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and trituration of crude residuewith MeOH (5 mL)1-(2-((3-amino-3-oxopropyl)(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(102b) (158 mg, 0.32 mmol, 47% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.89 (t, J=5.5 Hz) and 8.56 (t, J=5.8 Hz) (2t, 1H), 8.24-8.08(m, 1H), 7.78-7.65 (m, 1H), 7.64-6.85 (m, 9H), 5.70 and 5.412 (s, 2H),4.47 (d, J=5.5 Hz) and 4.38-4.24 (m) and 3.95 (s) (4H), 3.74 (t, J=6.3Hz) and 3.41 (t, J=7.0 Hz) (2t, 2H), 2.28 (t, J=7.1 Hz, 1H); ¹⁹F NMR(282 MHz, DMSO-d₆) δ −121.36, −121.65; MS (ES+) 489.5 (M+1); (ES−):487.4 (M−1); [based on NMR, this compound is a mixture of two rotamers4:5 ratio].

Preparation of2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)-N-(2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)-N-isopropylacetamide(103a)

Reaction of N-(6-bromopyridin-2-yl)-2-(isopropylamino)acetamide (28b)(61 mg, 0.23 mmol) with2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)acetic acid (97b) (70mg, 0.23 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column chromatography[silica gel (12 g), eluting with CMA80 in CHCl₃ 0 to 30%]2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)-N-(2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)-N-isopropylacetamide(103a) (45 mg, 0.080 mmol, 35% yield) as an off-white solid as a mixtureof rotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 11.20 and 10.83 (2s, 1H), 8.56and 8.55 (2s, 1H), 8.50 and 8.49 (2s, 1H), 8.47 and 8.46 (2s, 2H), 8.25and 8.24 (2s, 1H), 8.21-7.97 (m, 2H), 7.81 and 7.70 (2t, J=8.0 Hz, 1H),7.48-7.27 (m, 2H), 7.17-7.07 (m, 1H), 5.37 and 5.18 (2s, 2H), 4.71-4.59and 4.36-4.23 (2m, 1H), 4.43 and 4.05 (2s, 2H), 2.42 and 2.40 (2s, 3H),1.26 and 1.04 (2d, J=6.8 Hz, 6H); MS (ES+): 564.5, 566.5 (M+1), MS(ES−): 562.5, 564.5 (M−1), 598.5, 600.5 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((cis)-3-hydroxycyclobutyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(104b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-(((cis)-3-hydroxycyclobutyl)amino)acetamide(104a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (350 mg,1.48 mmol) with (cis)-3-aminocyclobutanol hydrochloride (458 mg, 3.71mmol) according to the procedure reported in step-2 of Scheme 35 gaveafter workup and purification by flash column chromatography [silica (12g), eluting with EtOAc/MeOH (9:1) in hexane 0 to 60%]N-(3-chloro-2-fluorobenzyl)-2-(((cis)-3-hydroxycyclobutyl)amino)acetamide(104a) (250 mg, 0.87 mmol, 59%) as a yellow oil; MS (ES+): 287.3 (M+1);MS (ES−): 285.3 (M−1).

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((cis-3-hydroxycyclobutyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(104b)

Reaction ofN-(3-chloro-2-fluorobenzyl)-2-(((cis)-3-hydroxycyclobutyl)amino)acetamide(104a) (250 mg, 0.87 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (210 mg, 0.96 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with CMA-80 in CHCl₃ 0 to 60%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((cis)-3-hydroxycyclobutyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(104b) (245 mg, 0.5 mmol, 58% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.88 (t, J=5.7 Hz) and 8.44 (t, J=5.9 Hz) (2t, 1H), 8.24-8.09(m, 1H), 7.70 (s, 1H), 7.59-7.04 (m, 7H), 5.53 and 5.40 (2s, 2H),5.20-5.06 (m, 1H), 4.47 (d, J=5.5 Hz) and 4.34 (d, J=5.7 Hz) (2d, 2H),4.30 and 4.04 (2s, 2H), 4.19-4.05 (m, 1H), 3.88-3.68 (m, 1H), 2.70-2.55(m, 1H), 2.39-2.25 (m, 1H), 2.13-1.90 (m, 1H), 1.85-1.70 (m, 1H); ¹⁹FNMR (282 MHz, DMSO-d₆) δ −121.26, −121.59; MS (ES+); 488.5 (M+1); (ES−):486.5 (M−1); [based on NMR, this compound is a mixture of rotamers 4:5ratio]

Preparation of2-(3-acetyl-5-(pyridin-3-yl)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(105a)

Reaction of2-(3-acetyl-5-bromo-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(90d) (150 mg, 0.28 mmol) with pyridin-3-ylboronic acid (34 mg, 0.28mmol) according the procedure reported in Scheme 100 gave after workupand purification by flash column chromatography [silica gel (12 g),eluting with CMA80 in CHCl₃ 0 to 30%]2-(3-acetyl-5-(pyridin-3-yl)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(105a) (75 mg, 0.14 mmol, 50% yield) as a white solid as a mixture ofrotamers in 2:1 ratio; ¹H NMR (300 MHz, DMSO-d₆) δ 8.91-8.87 (m, 1H),8.84 (t, J=5.7 Hz) and 8.39-8.27 (m) (2H), 8.61-8.53 (m, 1H), 8.45 (s,1H), 8.14-8.05 (m, 1H), 7.67-7.57 (m, 2H), 7.57-7.47 (m, 2H), 7.46-7.36(m, 1H), 7.26-6.94 (m, 1H), 5.41 and 5.22 (s, 2H), 4.66-4.53 and4.32-4.21 (m, 1H), 4.49 and 4.34 (d, J=5.8 Hz, 2H), 4.20 and 3.86 (s,2H), 2.47 and 2.45 (s, 3H), 1.27 and 1.01 (2d, J=6.4 Hz, 6H); ¹⁹F NMR(282 MHz, DMSO-d₆) δ −121.18, −121.77; MS (ES+) 535.6 (M+1), MS (ES−):569.5, 571.5 (M+Cl).

Preparation of2-(3-acetyl-5-(2-fluoropyridin-4-yl)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(106a)

Reaction of2-(3-acetyl-5-bromo-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(90d) (150 mg, 0.28 mmol) with 2-fluoropyridin-4-ylboronic acid (39 mg,0.28 mmol) according the procedure reported in Scheme 100 gave afterworkup and purification by flash column chromatography [silica gel (12g), eluting with CMA80 in CHCl₃ 0 to 30%]2-(3-acetyl-5-(2-fluoropyridin-4-yl)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(106a) (52 mg, 0.094 mmol, 34% yield) as a white solid as a mixture ofrotamers in 2:1 ratio; ¹H NMR (300 MHz, DMSO-d₆) δ 8.84 (t, J=5.7 Hz)and 8.42-8.23 (m) (3H), 8.58 (bs, 1H), 7.81-6.89 (m, 7H), 5.42 and 5.23(2s, 2H), 4.66-4.53 and 4.30-4.22 (m, 1H), 4.49 and 4.34 (2d, J=5.8 Hz,2H), 4.20 and 3.86 (s, 2H), 2.48 and 2.46 (s, 3H), 1.27 and 1.00 (2d,J=6.8 Hz, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −69.06, −69.09, −121.18,−121.77; MS (ES+): 553.6 (M+1), MS (ES−): 587.5 (M+Cl).

Preparation of2-(3-acetyl-5-(pyridin-3-ylamino)-1H-indol-1-yl)-N-(2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)-N-isopropylacetamide(107c) Step-1: Preparation of tert-butyl2-(3-acetyl-5-(pyridin-3-ylamino)-1H-indol-1-yl)acetate (107a)

Reaction of tert-butyl 2-(3-acetyl-5-bromo-1H-indol-1-yl)acetate (90b)(1.05 g, 2.98 mmol) with pyridin-3-amine (310 mg, 3.28 mmol), accordingto the procedure reported in step-1 of Scheme 97 gave after workup andpurification by column chromatography [silica gel (40 g), eluting withCMA80 in CHCl₃ 0 to 20%] tert-butyl2-(3-acetyl-5-(pyridin-3-ylamino)-1H-indol-1-yl)acetate (107a) (250 g,0.7 mmol, 23% yield) as light yellow solid; ¹H NMR (300 MHz, DMSO-d₆) δ8.35-8.23 (m, 3H), 8.02-7.91 (m, 2H), 7.43-7.31 (m, 2H), 7.18 (dd,J=8.3, 4.6 Hz, 1H), 7.07 (dd, J=8.8, 2.2 Hz, 1H), 5.08 (s, 2H), 2.41 (s,3H), 1.44 (s, 9H); MS (ES+): 366.5 (M+1), MS (ES−): 400.4 (M+Cl).

Step-2: Preparation of2-(3-acetyl-5-(pyridin-3-ylamino)-1H-indol-1-yl)acetic acid (107b)

Reaction of tert-butyl2-(3-acetyl-5-(pyridin-3-ylamino)-1H-indol-1-yl)acetate (107a) (250 mg,0.68 mmol) with TFA (1.58 mL, 20.52 mmol) according to the procedurereported in step-2 of Scheme 2 gave after workup and trituration ofcrude with EtOAc-hexane (10 mL)2-(3-acetyl-5-(pyridin-3-ylamino)-1H-indol-1-yl)acetic acid (107b) (0.2g, 0.647 mmol, 95% yield) as light orange solid; ¹H NMR (300 MHz,DMSO-d₆) δ 13.31 (bs, 1H, D₂O exchangeable), 9.09 (s, 1H), 8.36 (s, 1H),8.28 (s, 1H), 8.14 (s, 1H), 8.05 (s, 1H), 7.82 (s, 1H), 7.70 (s, 1H),7.55 (d, J=8.7 Hz, 1H), 7.18 (d, J=8.6 Hz, 1H), 5.14 (s, 2H), 2.42 (s,3H); MS (ES−): 308.3 (M−1).

Step-3: Preparation of2-(3-acetyl-5-(pyridin-3-ylamino)-1H-indol-1-yl)-N-(2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)-N-isopropylacetamide(107c)

Reaction of 2-(3-acetyl-5-(pyridin-3-ylamino)-1H-indol-1-yl)acetic acid(107b) (60 mg, 0.19 mmol) withN-(6-bromopyridin-2-yl)-2-(isopropylamino)acetamide (28b) (53 mg, 0.19mmol) according to the procedure reported in step-3 of Scheme 2 gaveafter workup and purification by flash column [silica gel (12 g),eluting with CMA-80 in CHCl₃ 0-100%]2-(3-acetyl-5-(pyridin-3-ylamino)-1H-indol-1-yl)-N-(2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)-N-isopropylacetamide(107c) (57 mg, 0.101 mmol, 52% yield) as a off-white solid as a mixtureof rotamers in 2:1 ratio; ¹H NMR (300 MHz, DMSO-d₆) (a mixture of tworotamers) δ 11.20 and 10.82 (2s, 1H), 8.33-8.24 (m, 2H), 8.22 and 8.21(2s, 1H), 8.05-7.91 (m, 3H), 7.81 and 7.70 (2t, J=8.0 Hz, 1H), 7.44-7.28(m, 3H), 7.23-7.11 (m, 1H), 7.12-7.01 (m, 1H), 5.35 and 5.16 (2s, 2H),4.72-4.57 and 4.47-4.20 (2m, 1H), 4.43 and 4.05 (2s, 2H), 2.41 and 2.40(2s, 3H), 1.26 and 1.04 (2d, J=6.8 Hz, 6H); MS (ES+): 563.5, 565.5(M+1); MS (ES−): 561.5, 563.5 (M−1), 597.5, 599.5 (M+Cl).

Preparation of2-(3-acetyl-5-(pyrimidin-5-yl)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(108a)

Reaction of2-(3-acetyl-5-bromo-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(90d) (150 mg, 0.28 mmol) with pyrimidin-5-ylboronic acid (35 mg, 0.28mmol) according the procedure reported in Scheme 100 gave after workupand purification by flash column chromatography [silica gel (12 g),eluting with CMA80 in CHCl₃ 0 to 30%]2-(3-acetyl-5-(pyrimidin-5-yl)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(108a) (85 mg, 0.159 mmol, 57% yield) as a white solid; as a mixture ofrotamers in 2:1 ratio; ¹H NMR (300 MHz, DMSO-d₆) (a mixture of tworotamers) δ 9.19 and 9.18 (2s, 1H), 9.12 and 9.11 (2s, 2H), 8.89-8.79and 8.40-8.28 (2m, 2H), 8.48 (s, 1H), 7.71-6.95 (m, 5H), 5.42 and 5.23(2s, 2H), 4.65-4.54 and 4.32-4.21 (2m, 1H), 4.49 and 4.34 (2d, J=5.6 Hz,2H), 4.20 and 3.86 (2s, 2H), 2.48 and 2.46 (2s, 3H), 1.27 and 1.01 (d,J=6.8 Hz, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) (a mixture of two rotamers) δ−121.18 and −121.79; MS (ES+): 536.5 (M+1), MS (ES−): 534.5 (M−1), 570.5(M+Cl).

Preparation of2-(3-acetyl-5-(3-acetylphenyl)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(109a)

Reaction of2-(3-acetyl-5-bromo-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(90d) (150 mg, 0.28 mmol) with1-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethanone (70mg, 0.28 mmol) according the procedure reported in Scheme 100 gave afterworkup and purification by flash column chromatography [silica gel (12g), eluting with CMA80 in CHCl₃ 0 to 30%]2-(3-acetyl-5-(3-acetylphenyl)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(109a) (80 mg, 0.14 mmol, 50% yield) as a white solid as mixture ofrotamers in 2:1 ratio; ¹H NMR (300 MHz, DMSO-d₆) δ 8.84 and 8.35 (2t,J=5.7 Hz, 1H), 8.47 (bs, 1H), 8.35 and 8.34 (s, 1H), 8.21-8.13 (m, 1H),8.01-7.88 (m, 2H), 7.70-6.95 (m, 6H), 5.41 and 5.22 (s, 2H), 4.68-4.51and 4.32-4.20 (m, 1H), 4.49 and 4.34 (d, J=5.8 Hz, 2H), 4.20 and 3.86(s, 2H), 2.668 and 2.666 (2s, 3H), 2.47, 2.45 (s, 3H), 1.27 and 1.01(2d, J=6.8 Hz, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.18, −121.76; MS(ES+): 576.6 (M+1), 598.6 (M+Na); MS (ES−): 574.6 (M−1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((trans)-3-hydroxycyclobutyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(110b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-(((trans)-3-hydroxycyclobutyl)amino)acetamide(110a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (350 mg,1.48 mmol) with (trans)-3-aminocyclobutanol hydrochloride (458 mg, 3.71mmol) according to the procedure reported in step-2 of Scheme 35 gaveafter workup and purification by flash column chromatography [silica (12g), eluting with EtOAc/MeOH (9:1) in hexane 0 to 60%]N-(3-chloro-2-fluorobenzyl)-2-(((trans)-3-hydroxycyclobutyl)amino)acetamide(110a) (200 mg, 0.7 mmol, 47%) as a yellow oil; MS (ES+): 287.4 (M+1);(ES−): 285.3 (M−1).

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((trans)-3-hydroxycyclobutyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(110b)

Reaction ofN-(3-chloro-2-fluorobenzyl)-2-(((trans)-3-hydroxycyclobutyl)amino)acetamide(110a) (200 mg, 0.7 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (168 mg, 0.77 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with CMA-80 in CHCl₃ 0 to 60%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((trans)-3-hydroxycyclobutyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(110b) (92 mg, 27%) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 8.86(t, J=5.5 Hz) and 8.43 (t, J=5.7 Hz) (2t, 1H), 8.18 (d, J=8.1 Hz, 1H),7.78-7.64 (m, 1H), 7.63-7.00 (m, 7H), 5.53 and 5.42 (2s, 2H), 5.12 (d,J=4.0 Hz) and 5.00 (d, J=4.3 Hz) (2d, 1H), 4.96-4.79 (m, 1H), 4.47 (d,J=5.2 Hz) and 4.33 (d, J=5.5 Hz) (2d, 2H), 4.28 and 4.00 (2s, 2H),4.23-4.05 (m, 1H), 2.46-2.30 (m, 1H), 2.28-2.09 (m, 2H), 2.02-1.85 (m,1H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.23, −121.62; MS (ES+): 488.5(M+1); (ES−): 486.5 (M−1); [based on NMR, this compound is a mixture ofrotamers 4:5 ratio].

Preparation of2-(3-acetyl-5-(pyridin-3-ylamino)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(111a)

Reaction of N-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide(19c) (50 mg, 0.19 mmol) with2-(3-acetyl-5-(pyridin-3-ylamino)-1H-indol-1-yl)acetic acid (107b) (60mg, 0.19 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column chromatography[silica gel (12 g), eluting with CMA80 in CHCl₃ 0 to 30%]2-(3-acetyl-5-(pyridin-3-ylamino)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(111a) (40 mg, 0.073 mmol, 38% yield) as an off-white solid as mixtureof rotamers in 2:1 ratio; ¹H NMR (300 MHz, DMSO-d₆) (a mixture of tworotamers) δ 8.82 and 8.34 (2t, J=5.7 Hz, 1H), 8.32-8.23 (m, 2H), 8.21and 8.16 (2s, 1H), 7.98 (d, J=2.2 Hz, 1H), 7.96-7.90 (m, 1H), 7.56-6.96(m, 7H), 5.32 and 5.13 (2s, 2H), 4.67-4.51 and 4.31-4.18 (2m, 1H), 4.47and 4.34 (2d, J=5.8 Hz, 2H), 4.18 and 3.85 (2s, 2H), 2.40 and 2.39 (2s,3H), 1.25 and 1.00 (2d, J=6.8 Hz, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) (amixture of two rotamers) δ −121.18, −121.77; MS (ES+): 550.6 (M+1); MS(ES−): 584.6 (M+Cl).

Preparation of2-(3-acetyl-5-(pyrimidin-5-ylethynyl)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(112a)

Reaction of2-(3-acetyl-5-bromo-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(90d) (300 mg, 0.56 mmol) with 5-ethynylpyrimidine (58 mg, 0.56 mmol)according to the procedure reported in Scheme 92 gave after workup andpurification by flash column chromatography [First column: silica gel(24 g), eluting with MeOH in CHCl₃ 0 to 20%; Second column: silica gel(12 g), eluting with MeOH/EtOAc (9:1) in hexanes 0 to 100%]2-(3-acetyl-5-(pyrimidin-5-ylethynyl)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(112a) (13 mg, 0.023 mmol, 4% yield) as a yellow solid as a mixture oftwo rotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 9.183 and 9.180 (2s, 1H),9.054 and 9.052 (2s, 2H), 8.84 (t, J=5.8 Hz) and 8.36 (t) (2t, 1H), 8.45(d, J=1.5 Hz, 1H), 8.38 and 8.34 (2s, 1H), 7.68-6.93 (m, 5H), 5.41 and5.22 (2s, 2H), 4.65-4.53 and 4.28-4.20 (2m, 1H), 4.52-4.30 (m, 2H), 4.19and 3.85 (2s, 2H), 2.46 and 2.45 (2s, 3H), 1.26 (d, J=6.5 Hz) and 1.00(d, J=6.8 Hz) (2t, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.18, −121.77;MS (ES+): 560.61 (M+1); MS (ES−): 594.5 & 596.5 (M+Cl).

Preparation of2-(3-acetyl-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(113b)

Reaction of N-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide(19c) (400 mg, 1.55 mmol) with 2-(3-acetyl-1H-indol-1-yl)acetic acid(113a) (403 mg, 1.86 mmol) according to the procedure reported in step-3of Scheme 2 gave after workup and purification by flash columnchromatography [silica gel (24 g), eluting with CMA80 in CHCl₃ 0 to 10%]2-(3-acetyl-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(113b) (279 mg, 0.609 mmol, 39% yield) as a pale yellow solid in theform of mixture of two rotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 8.82 and8.35 (t, J=5.4 Hz) (2t, 1H), 8.32 and 8.27 (2s, 1H), 8.22 (s, 1H), 8.18(d, J=7.0 Hz, 1H), 7.57-7.34 (m, 2H), 7.29-7.14 (m, 2H, another tripletwas overlapped in this region), 7.00 (t, J=7.9 Hz, 1H), 5.36 and 5.17(2s, 2H), 4.65-4.52 and 4.30-4.22 (2m, 1H), 4.48 (d, J=5.6 Hz) and 4.33(d, J=5.8 Hz) (2d, 2H), 4.19 (s) and 3.85 (2s, 2H), 2.43 and 2.42 (2s,3H), 1.25 (d, J=6.3 Hz) and 1.00 (d, J=6.8 Hz) (2d, 6H); ¹⁹F NMR (282MHz, DMSO-d₆) δ −121.19, −121.82; MS (ES+): 458.5 (M+1), 480.5 (M+Na);MS (ES−): 456.5 (M−1), 492.5 (M+Cl).

Preparation of2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-((trans)-3-hydroxycyclobutyl)acetamide(114a)

Reaction ofN-(3-chloro-2-fluorobenzyl)-2-(((trans)-3-hydroxycyclobutyl)amino)acetamide(110a) (55 mg, 0.19 mmol) with2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)acetic acid (97b) (60mg, 0.19 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column chromatography[silica gel (12 g), eluting with CMA80 in CHCl₃ 0 to 100%]2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-((trans)-3-hydroxycyclobutyl)acetamide(114a) (12 mg, 0.021 mmol, 11% yield) as a white solid as a mixture ofrotamers in 2:1 ratio; ¹H NMR (300 MHz, DMSO-d₆) δ 8.85 and 8.42 (2t,J=5.6 Hz, 1H), 8.563 and 8.559 (2s, 1H), 8.49 (s, 1H), 8.46 (s, 2H),8.22 and 8.17 (2s, 1H), 8.004 and 7.997 (2s, 1H), 7.58-7.01 (m, 5H),5.29 (s) and 5.17-4.79 (m) (s & m, 4H), 4.47 and 4.35 (2d, J=5.8 Hz,2H), 4.27 and 4.02 (2s, 2H), 4.24-4.09 (m, 1H), 2.41 and 2.40 (2s, 3H),2.28-2.11 (m, 2H), 2.00-1.84 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.20, −121.62; MS (ES+): 579.6 (M+1), MS (ES−): 613.5, 615.5 (M+Cl).

Preparation of2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)-N-(2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)-N-isopropylacetamide(115d) Step-1: Preparation of2-chloro-N-(2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)acetamide (115b)

To a biphasic solution of 2′-chloro-2-fluorobiphenyl-3-amine (115a) (0.8g, 3.61 mmol, prepared according to procedure reported by Altmann, Evaet al, in PCT Int. Appl., WO 2012/093101) in EtOAc (20 mL), Saturatedaqueous NaHCO₃ (20 mL) was added 2-chloroacetyl chloride (35a) (0.58 mL,7.22 mmol) and stirred at RT for 2 h. The layers were separated andaqueous layer was extracted with EtOAc (40 mL). The organic layers werecombined washed with brine, dried, filtered and concentrated in vacuumto afford 2-chloro-N-(2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)acetamide(115b) (1 gm, 93% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ10.24 (s, 1H), 8.00 (t, J=7.9 Hz, 1H), 7.64-7.57 (m, 1H), 7.53-7.39 (m,3H), 7.28 (td, J=8.0, 1.0 Hz, 1H), 7.19-7.07 (m, 1H), 4.37 (s, 2H); MS(ES+): 298.3, 300.3 (M+1), 320.3, 322.3 (M+Na); MS (ES−): 296.3, 298.3(M−1).

Step-2: Preparation ofN-(2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-2-(isopropylamino)acetamide(115c)

To a solution of 2-chloro-N-(2′-chloro-2-fluorobiphenyl-3-yl)acetamide(115b) (1.00 g, 3.35 mmol) in THF (30 mL) was added isopropylamine (0.86mL, 10.06 mmol) and stirred at RT for 24h. Reaction mixture was pouredinto saturated aqueous NaHCO₃ solution (60 mL) and extracted with EtOAc(2×50 mL). The organics layers were combined washed with brine, dried,filtered, concentrated and purified by flash column chromatography[silica gel (24 g), eluting with EtOAc in Hexane 0 to 100%] to affordN-(2′-chloro-2-fluorobiphenyl-3-yl)-2-(isopropylamino)acetamide (115c)(520 mg, 1.62 mmol, 48% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) (major rotamer) δ 8.25 (td, J=7.8, 1.7 Hz, 1H), 7.65-7.56 (m,1H), 7.53-7.37 (m, 4H), 7.27 (td, J=8.0, 1.1 Hz, 1H), 7.11-7.02 (m, 1H),3.30 (s, 2H), 2.79-2.66 (m, 1H), 1.04-0.94 (m, 6H); MS (ES+) 321.4,323.4 (M+1), MS (ES−): 355.3, 357.3 (M+Cl).

Step-3: Preparation of2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)-N-(2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)amino)-2-oxoethyl)-N-isopropylacetamide(115d)

Reaction ofN-(2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-2-(isopropylamino)acetamide(115c) (62 mg, 0.19 mmol) with2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)acetic acid (97b) (60mg, 0.19 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column chromatography[silica gel (12 g), eluting with CMA80 in CHCl₃ 0 to 30%]2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)-N-(2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)-N-isopropylacetamide(115d) (21m g, 0.034 mmol, 18% yield) as a white solid as a mixture ofrotamers in 2:1 ratio; ¹H NMR (300 MHz, DMSO-d₆) (a mixture of tworotamers) δ 10.25 and 9.74 (2s, 1H), 8.56 (s, 1H), 8.52-8.43 (m, 3H),8.26 and 8.24 (s, 1H), 8.15-7.91 (m, 2H), 7.66-7.36 (m, 4H), 7.32 and7.22 (2t, J=8.0 Hz, 1H), 7.18-7.02 (m, 2H), 5.38 and 5.21 (2s, 2H),4.75-4.59 and 4.38-4.23 (2m, 1H), 4.47 and 4.10 (2s, 2H), 2.42 and 2.40(2s, 3H), 1.28 and 1.07 (2d, J=6.8 Hz, 6H); MS (ES+); 613.5, 615.7(M+1), MS (ES−); 611.6, 613.6 (M−1).

Preparation of2-(3-acetyl-5-(pyrimidin-2-ylethynyl)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(116a)

Reaction of2-(3-acetyl-5-bromo-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(90d) (325 mg, 0.61 mmol) with 2-ethynylpyrimidine (63 mg, 0.61 mmol)according to the procedure reported in scheme 92 gave after workup andpurification by flash column chromatography [silica gel (12 g), elutingwith EtOAc/MeOH (9:1) in hexanes 0 to 100%]2-(3-acetyl-5-(pyrimidin-2-ylethynyl)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(116a) (14 mg, 0.025 mmol, 4% yield) as a dark-yellow solid in the formof mixture of two rotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 8.92-8.80 (m,2H), 8.59 (t, J=5.0 Hz) and 8.42-8.29 (m) (t & m, 2H), 8.51-8.45 (m,1H), 7.66-6.93 (m, 6H), 5.42 and 5.24 (2s, 2H), 4.67-4.55 and 4.29-4.24(2m, 1H), 4.52-4.31 (m, 2H), 4.19 and 3.86 (2s, 2H), 2.47 and 2.46 (2s,3H), 1.27 (d, J=6.4 Hz) and 1.01 (d, J=6.8 Hz) (2d, 6H); ¹⁹F NMR (282MHz, DMSO-d₆) δ −121.17, −121.75; MS (ES+): 560.6 (M+1); MS (ES−): 558.5& 560.6 (M−1).

Preparation of2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorophenyl)amino)-2-oxoethyl)-N-isopropylacetamide(117e) Step-1: Preparation of tert-butyl2-(2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)-N-isopropylacetamido)acetate(117b)

Reaction of tert-butyl 2-(isopropylamino)acetate (117a) (134 mg, 0.77mmol, prepared according to the procedure reported by Brotherton-Pleiss,Christine E. et al; in PCT Int. Appl., 2014049047) with2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)acetic acid (97b) (160mg, 0.52 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column chromatography[silica gel (12 g), eluting with CMA80 in CHCl₃ 0 to 30%] tert-butyl2-(2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)-N-isopropylacetamido)acetate(117b) (120 mg, 0.26 mmol, 50% yield) as an off-white solid; ¹H NMR (300MHz, DMSO-d₆) δ 8.56 (d, J=0.9 Hz, 1H), 8.49 (s, 1H), 8.47 (s, 1H), 8.46(s, 1H), 8.24 (s, 1H), 8.01 (d, J=2.1 Hz, 1H), 7.33 (t, J=8.2 Hz, 1H),7.16-7.06 (m, 1H), 5.36 and 5.05 (2s, 2H), 4.67-4.52 and 4.34-4.27 (m,1H), 4.26 and 3.84 (2s, 2H), 2.42 and 2.41 (2s, 3H), 1.51 and 1.36 (2s,9H), 1.22 and 1.04 (2d, J=6.8 Hz, 6H); MS (ES−) 464.5 (M−1).

Step-2: Preparation of2-(2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)-N-isopropylacetamido)aceticacid (117c)

Reaction of tert-butyl2-(2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)-N-isopropylacetamido)acetate(117b) (120 mg, 0.26 mmol) with TFA (0.4 mL, 5.16 mmol) according to theprocedure reported in step-2 of Scheme 2 gave after workup2-(2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)-N-isopropylacetamido)aceticacid (117c) (120 mg, 0.29 mmol, 114% yield) light orange gummy solid; ¹HNMR (300 MHz, DMSO-d₆) δ 8.57 (s, 1H), 8.48 (s, 2H), 8.25 (d, J=1.3 Hz,1H), 8.01 (t, J=2.2 Hz, 1H), 7.36 and 7.34 (2s, 1H), 7.12 and 7.09 (2t,J=1.9 Hz, 1H), 5.35 and 5.07 (s, 2H), 4.66-4.54 (m, 1H), 4.35-4.18 (m,1H), 3.87 (s, 1H), 2.41 and 2.41 (2s, 3H), 1.23 and 1.04 (2d, J=6.8 Hz,6H); MS (ES+) 410.5 (M+1); MS (ES−) 408.5 (M−1).

Step-3: Preparation of2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorophenyl)amino)-2-oxoethyl)-N-isopropylacetamide(117e)

Reaction of2-(2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)-N-isopropylacetamido)aceticacid (117c) (50 mg, 0.12 mmol) with 3-chloro-2-fluoroaniline (117d)(0.018 g, 0.122 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup and purification by flash columnchromatography [silica gel (12 g), eluting with CMA80 in CHCl₃ 0 to 30%]2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorophenyl)amino)-2-oxoethyl)-N-isopropylacetamide(117e) (25 mg, 0.047 mmol, 38% yield) as an off-white solid as a mixtureof two rotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 10.33 and 9.84 (2s, 1H),8.56 (s, 1H), 8.49 (s, 1H), 8.47 and 8.46 (2s, 2H), 8.25 and 8.23 (2s,1H), 8.03-8.00 (m, 1H), 7.97 and 7.79 (2t, J=7.6 Hz, 1H), 7.49-7.06 (m,4H), 5.38 and 5.19 (2s, 2H), 4.75-4.58 and 4.37-4.25 (2m, 1H), 4.46 and4.09 (2s, 2H), 2.42 and 2.41 (2s, 3H), 1.28 and 1.07 (2d, J=6.8 Hz, 6H);¹⁹F NMR (282 MHz, DMSO-d₆) (a mixture of two rotamers) δ −126.50,−126.67; MS (ES+): 537.6 (M+1); MS (ES−): 535.5 (M−1).

Preparation of2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)-N-(2-(((6-bromopyridin-2-yl)methyl)amino)-2-oxoethyl)-N-isopropylacetamide(118b)

Reaction of2-(2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)-N-isopropylacetamido)aceticacid (117c) (60 mg, 0.15 mmol) with (6-bromopyridin-2-yl)methanamine(118a) (27 mg, 0.15 mmol) according to the procedure reported in step-3of Scheme 2 gave after workup and purification by flash columnchromatography [silica gel (12 g), eluting with CMA80 in CHCl₃ 0 to 30%]2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)-N-(2-(((6-bromopyridin-2-yl)methyl)amino)-2-oxoethyl)-N-isopropylacetamide(118b) (5 mg, 0.086 mmol, 59% yield) as an off-white solid as a mixtureof two rotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 8.92 (t, J=6.0 Hz, 1H),8.56 and 8.55 (2s, 1H), 8.48 (s, 1H), 8.464 and 8.458 (2s, 2H), 8.24 and8.19 (2s, 1H), 8.00 (t, 1H), 7.74 (t, J=7.7 Hz, 1H), 7.62-7.19 (m, 3H),7.13-7.00 (m, 1H), 5.34 and 5.17 (2s, 2H), 4.67-4.54 and 4.28-4.24 (2m,1H), 4.48 and 4.34 (2d, J=6.0 Hz, 2H), 4.22 and 3.87 (2s, 2H), 2.40 and2.39 (2s, 3H), 1.28 and 1.04 (d, J=6.8 Hz, 6H); MS (ES+): 578.6, 580.6(M+1); MS (ES−): 576.6, 578.5 (M−1).

Preparation of(S)-1-(2-(sec-butyl(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(119b) Step-1: Preparation of(S)-2-(sec-butylamino)-N-(3-chloro-2-fluorobenzyl)acetamide (119a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (350 mg,1.48 mmol) with (S)-butan-2-amine (271 mg, 3.71 mmol) according to theprocedure reported in step-2 of Scheme 35 gave after workup(S)-2-(sec-butylamino)-N-(3-chloro-2-fluorobenzyl)acetamide (119a) (402mg, 1.47 mmol, 99% yield) as a yellow oil, which was used in the nextstep without further purification; ¹H NMR (300 MHz, DMSO-d₆) δ 8.35 (t,J=5.8 Hz, 1H), 7.52-7.38 (m, 1H), 7.33-7.23 (m, 1H), 7.23-7.09 (m, 1H),4.37 (d, J=5.9 Hz, 2H), 3.13 (s, 2H), 2.46-2.31 (m, 1H), 2.07 (s, 1H),1.55-1.30 (m, 1H), 1.30-1.08 (m, 1H), 0.92 (d, J=6.3 Hz, 3H), 0.81 (t,J=7.4 Hz, 3H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.65; MS (ES⁺) 273.4(M+1); MS (ES⁻) 271.3 (M−1);

Step-2: Preparation of(S)-1-(2-(sec-butyl(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(119b)

Reaction of (S)-2-(sec-butylamino)-N-(3-chloro-2-fluorobenzyl)acetamide(119a) (180 mg, 0.66 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (159 mg, 0.73 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with CMA-80 in CHCl₃ 0 to 60%](S)-1-(2-(sec-butyl(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide (119b) (220 mg, 0.46 mmol, 70% yield)as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 8.82 (t, J=5.7 Hz) and8.35 (t, J=5.9 Hz) (2t, 1H), 8.18 (d, J=8.1 Hz, 1H), 7.75-7.67 (m, 1H),7.61-7.00 (m, 7H), 5.68-5.39 (m, 2H), 4.51-3.70 (m, 5H), 1.63-0.50 (m,8H); ¹⁹F NMR (282 MHz, DMSO) δ −121.19, −121.76; MS (ES+): 474.5 (M+1),496.5 (M+Na); (ES−): 472.5 (M−1); 518.5 (M+Cl); [based on NMR, thiscompound is a mixture of two rotamers 2:1 ratio].

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(pentan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(120b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-(pentan-2-ylamino)acetamide (120a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (350 mg,1.48 mmol) with pentan-2-amine (323 mg, 3.71 mmol) according to theprocedure reported in step-2 of Scheme 35 gave after workupN-(3-chloro-2-fluorobenzyl)-2-(pentan-2-ylamino)acetamide (120a) (400mg, 1.4 mmol, 94% yield) as a yellow oil, which was used in the nextstep without further purification; ¹H NMR (300 MHz, DMSO-d₆) δ 8.36 (t,J=6.0 Hz, 1H), 7.53-7.42 (m, 1H), 7.34-7.24 (m, 1H), 7.22-7.11 (m, 1H),4.37 (d, J=5.8 Hz, 2H), 3.14 (d, J=2.6 Hz, 2H), 2.50-2.42 (m, 1H), 2.06(s, 1H), 1.40-1.14 (m, 4H), 0.93 (d, J=6.3 Hz, 3H), 0.84 (t, J=7.0 Hz,3H); ¹⁹F NMR (282 MHz, DMSO) δ −121.65; MS (ES+) 287.4 (M+1); MS (ES−)285.4 (M−1);

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(pentan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(120b)

Reaction of N-(3-chloro-2-fluorobenzyl)-2-(pentan-2-ylamino)acetamide(120a) (146 mg, 0.51 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (123 mg, 0.56 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with CMA-80 in CHCl₃ 0 to 60%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(pentan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(120b) (174 mg, 0.36 mmol, 70% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.81 (t, J=5.7 Hz) and 8.35 (t, J=5.9 Hz) (2t, 1H), 8.18 (d,J=8.1 Hz, 1H), 7.71 (s, 1H), 7.57-7.10 (m, 7H), 5.66-5.35 (m, 2H),4.63-3.67 (m, 5H), 1.45-0.69 (m, 10H); ¹⁹F NMR (282 MHz, DMSO) δ−121.19, −121.75; MS (ES+): 488.5 (M+1), 510.5 (M+Na); (ES−): 486.5(M−1). [based on NMR, this compound is a mixture of two rotamers with3:1 ratio]

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(4-methylpentan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(121b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-((4-methylpentan-2-yl)amino)acetamide(121a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (350 mg,1.48 mmol) with 4-methylpentan-2-amine (375 mg, 3.71 mmol) according tothe procedure reported in step-2 of Scheme 35 gave after workup andpurification by flash column chromatography [silica (12 g), eluting withEtOAc/MeOH (9:1) in hexane 0 to 60%] to giveN-(3-chloro-2-fluorobenzyl)-2-(4-methylpentan-2-ylamino)acetamide (121a)(235 mg, 0.78 mmol, 53% yield) as a yellow oil; ¹H NMR (300 MHz,DMSO-d₆) δ 8.35 (t, J=6.0 Hz, 1H), 7.55-7.41 (m, 1H), 7.37-7.25 (m, 1H),7.22-7.12 (m, 1H), 4.45-4.29 (m, 2H), 3.14 (d, J=3.9 Hz, 2H), 2.54-2.49(m, 1H), 2.06 (s, 1H), 1.75-1.51 (m, 1H), 1.35-1.13 (m, 1H), 1.13-0.98(m, 1H), 0.92 (d, J=6.2 Hz, 3H), 0.86-0.77 (m, 6H); ¹⁹F NMR (282 MHz,DMSO) δ −121.63; MS (ES+): 301.4 (M+1); MS (ES−): 299.4 (M−1);

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(4-methylpentan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(121b)

Reaction ofN-(3-chloro-2-fluorobenzyl)-2-(4-methylpentan-2-ylamino)acetamide (121a)(120 mg, 0.4 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e)(96 mg, 0.44 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with CMA-80 in CHCl₃ 0 to 60%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(4-methylpentan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(121b) (142 mg, 0.28 mmol, 71% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.81 (t, J=5.7 Hz) and 8.36 (t, J=6.2 Hz) (2t, 1H), 8.25-8.11(m, 1H), 7.72 (s, 1H), 7.57-7.17 (m, 7H), 5.78-5.25 (m, 2H), 4.66-4.02(m, 5H), 1.56-0.63 (m, 12H); ¹⁹F NMR (282 MHz, DMSO) δ −121.17, −121.72;MS (ES+) 524.6 (M+Na); (ES−): 500.5 (M−1); [based on NMR, this compoundis a mixture of two rotamers 4:1 ratio].

Preparation of(R)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-cyclopropylethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(122b) Step-1: Preparation of(R)—N-(3-chloro-2-fluorobenzyl)-2-((1-cyclopropylethyl)amino)acetamide(122a)

Reaction of 2-bromo-N-(3-chloro-2-fluorobenzyl)acetamide (69b) (323 mg,1.16 mmol) with (R)-1-cyclopropylethanamine (99 mg, 1.16 mmol) accordingto the procedure reported in step-2 of Scheme 35 gave after workup(R)—N-(3-chloro-2-fluorobenzyl)-2-((1-cyclopropylethyl)amino)acetamide(122a) (310 mg, 1.09 mmol, 94% yield) as a yellow oil which was used assuch without further purification; MS (ES+): 285.4 (M+1).

Step-2: Preparation of(R)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-cyclopropylethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(122b)

Reaction of(R)—N-(3-chloro-2-fluorobenzyl)-2-((1-cyclopropylethyl)amino)acetamide(122a) (310 mg, 1.09 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (286 mg, 1.31 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (40 g), eluting with MeOH in CHCl₃ 0 to 10%](R)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-cyclopropylethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(122b) (0.251 g, 0.517 mmol, 47.4% yield) as a white solid as a mixturetwo rotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 8.82 (t, J=5.7 Hz) and 8.29(t, J=5.9 Hz) (2t, 1H), 8.23-8.12 (m, 1H), 7.73 and 7.69 (2s, 1H),7.59-6.96 (m, 7H), 5.68-5.39 (m, 2H), 4.46 (d, J=5.5 Hz) and 4.39-4.26(m) and 3.96 (s) (d & m & s, 4H), 3.80-3.62 and 3.60-3.46 (2m, 1H), 1.27(d, J=6.4 Hz) and 1.03 (d, J=6.8 Hz) (2d, 3H), 1.15-0.79 (m, 1H),0.61-0.00 (m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.19, −121.75; MS(ES+): 486.5, 488.5 (M+1), 508.5, 510.5 (M+Na); MS (ES−): 484.5 (M−1),520.5, 522.5 (M+Cl).

Preparation of(S)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-cyclopropylethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(123b) Step-1: Preparation of(S)—N-(3-chloro-2-fluorobenzyl)-2-((1-cyclopropylethyl)amino)acetamide(123a)

Reaction of 2-bromo-N-(3-chloro-2-fluorobenzyl)acetamide (69b) (355 mg,1.27 mmol) with (S)-1-cyclopropylethanamine (108 mg, 1.27 mmol)according to the procedure reported in step-2 of Scheme 35 gave afterworkup(S)—N-(3-chloro-2-fluorobenzyl)-2-((1-cyclopropylethyl)amino)acetamide(123a) (354 mg, 1.24 mmol, 98% yield) as a thick yellow oil which wasused as such in the next step; MS (ES+): 285.4 (M+1); MS (ES−): 319.3(M+Cl)

Step-2: Preparation of(S)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-cyclopropylethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(123b)

Reaction of(S)—N-(3-chloro-2-fluorobenzyl)-2-((1-cyclopropylethyl)amino)acetamide(123a) (350 mg, 1.23 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (323 mg, 1.48 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [First column: Silica gel, (24 g) eluting with MeOH inDCM from 0-20%; Second column silica gel, (24 g) eluting with MeOH inCHCl₃ from 0-10%)](S)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-cyclopropylethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(123b) (0.079 g, 0.163 mmol, 13% yield) as a white solid in the form ofmixture two rotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 8.83 (t, J=5.7 Hz) and8.30 (t, J=5.9 Hz) (2t, 1H), 8.21-8.15 (m, 1H), 7.73 and 7.70 (2s, 1H),7.62-6.96 (m, 7H), 5.70-5.36 (m, 2H), 4.46 (d, J=5.5 Hz) and 4.36-4.26(m) and 3.97 (s) (d & m & s, 4H), 3.80-3.63 and 3.59-3.45 (2m, 1H), 1.28(d, J=6.5 Hz) and 1.03 (d, J=6.8 Hz)(2d, 3H), 1.15-0.79 (m, 1H), 0.60 to−0.02 (m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.19, −121.75. MS (ES+):486.5 (M+1), 508.5 (M+Na); MS (ES−): 484.5 & 486.5 (M−1), 520.5 (M+Cl).

Preparation of5-bromo-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indole-3-carboxamide(124e) Step-1: Preparation of 5-bromo-1H-indole-3-carboxamide (124b)

Reaction of 5-bromo-1H-indole-3-carbonitrile (124a) (1.38 g, 6.22 mmol)with ammonium hydroxide (4.85 mL, 124 mmol) and hydrogen peroxide (1.9mL, 62.2 mmol) according to the procedure reported Scheme 65 gave afterworkup 5-bromo-1H-indole-3-carboxamide (124b) (1.2 g, 5.02 mmol, 81%yield) as an off-white solid; MS (ES+): 239.2, 241.2 (M+2), MS (ES−):237.1, 239.1 (M−2).

Step-2: Preparation of tert-butyl2-(5-bromo-3-carbamoyl-1H-indol-1-yl)acetate (124c)

Reaction of 5-bromo-1H-indole-3-carboxamide (124b) (1.2 g, 5.02 mmol)with tert-butyl 2-bromoacetate (1.11 mL, 7.53 mmol) using potassiumcarbonate (1.39 g, 10.04 mmol) as base according to the procedurereported step-1 of Scheme 45 gave after workup and purification by flashcolumn chromatography [silica gel (40 g), eluting with CMA80 in CHCl₃ 0to 15%] tert-butyl 2-(5-bromo-3-carbamoyl-1H-indol-1-yl)acetate (124c)(970 mg, 2.75 mmol, 55% yield) as off-white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.36-8.27 (m, 1H), 8.00 (s, 1H), 7.54 (brs, 1H), 7.43 (dd,J=8.8, 0.6 Hz, 1H), 7.33 (dd, J=8.7, 2.0 Hz, 1H), 6.96 (brs, 1H), 5.10(s, 2H), 1.42 (s, 9H); MS (ES+): 353.4, 355.4 (M+2), MS (ES−): 351.3,353.3 (M−1).

Step-3: Preparation of 2-(5-bromo-3-carbamoyl-1H-indol-1-yl)acetic acid(124d)

Reaction of tert-butyl 2-(5-bromo-3-carbamoyl-1H-indol-1-yl)acetate(124c) (500 mg, 1.42 mmol) with TFA (2.18 mL, 28.3 mmol) according tothe procedure reported in step-2 of Scheme 2 gave after workup andtrituration of crude product with 30% EtOAc-hexane (10 mL)2-(5-bromo-3-carbamoyl-1H-indol-1-yl)acetic acid (124d) (420 mg, 1.41mmol, 100% yield) as light orange solid; ¹H NMR (300 MHz, DMSO-d₆) δ13.24 (bs, 1H), 8.31 (d, J=1.9 Hz, 1H), 8.01 (s, 1H), 7.65-7.38 (m, 2H),7.32 (dd, J=8.7, 2.0 Hz, 1H), 6.97 (s, 1H), 5.10 (s, 2H); MS (ES+):297.2, 299.3 (M+2); MS (ES−); 295.2, 297.2 (M−2).

Step-4: Preparation of5-bromo-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indole-3-carboxamide(124e)

Reaction of 2-(5-bromo-3-carbamoyl-1H-indol-1-yl)acetic acid (124d) (400mg, 1.35 mmol) withN-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide (19c) (348 mg,1.35 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup5-bromo-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indole-3-carboxamide(124e) (0.52 g, 0.967 mmol, 71.8% yield) as a white solid as a mixtureof two rotamers; ¹H NMR (300 MHz, DMSO-d₆) (a mixture of two rotamers) δ8.81 (t, J=5.7 Hz) and 8.34-8.27 (m) (t & m, 2H), 7.97 (s, 1H),7.59-6.76 (m, 7H), 5.32 and 5.14 (2s, 2H), 4.62-4.51 and 4.28-4.21 (2m,1H), 4.46 and 4.32 (2d, J=5.6 Hz, 2H), 4.15 and 3.83 (2s, 2H), 1.23 and0.98 (2d, J=6.8 Hz, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) (a mixture of tworotamers) δ −121.22 and −121.76; MS (ES+): 561.4 (M+23), MS (ES−):571.4, 573.3 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(pyrimidin-5-yl)-1H-indole-3-carboxamide(125a)

Reaction of5-bromo-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indole-3-carboxamide(124e) (120 mg, 0.22 mmol) with pyrimidin-5-ylboronic acid (33 mg, 0.27mmol) according the procedure reported in Scheme 100 gave after workupand purification by flash column chromatography [silica gel (12 g),eluting with CMA80 in CHCl₃ 0 to 30%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(pyrimidin-5-yl)-1H-indole-3-carboxamide(125a) as a white solid as a mixture of rotamers in 2:1 ratio; ¹H NMR(300 MHz, DMSO-d₆) δ 9.167 and 9.161 (2s, 1H), 9.138 and 9.131 (2s, 2H),8.83 and 8.33 (2t, J=5.7 Hz, 1H), 8.45 (s, 1H), 8.01 and 7.99 (2s, 1H),7.74-6.80 (m, 7H), 5.37 and 5.19 (2s, 2H), 4.65-4.53 and 4.31-4.20 (2m,1H), 4.48 and 4.33 (2d, J=5.6 Hz, 2H), 4.18 and 3.85 (2s, 2H), 1.25 and1.00 (2d, J=6.6 Hz, 6H); NMR (282 MHz, DMSO-d₆) δ −121.21 and −121.79;MS (ES+) 537.5 (M+1), 559.5 (M+23), MS (ES−) 571.5 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(2-(dimethylamino)pyrimidin-5-yl)-1H-indole-3-carboxamide(126a)

Reaction of5-bromo-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indole-3-carboxamide(124e) (120 mg, 0.22 mmol) with 2-(dimethylamino)pyrimidin-5-ylboronicacid (45 mg, 0.27 mmol) according the procedure reported in Scheme 100gave after workup and purification by flash column chromatography[silica gel (12 g), eluting with CMA80 in CHCl₃ 0 to40%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(2-(dimethylamino)pyrimidin-5-yl)-1H-indole-3-carboxamide(126a) (85 mg, 0.15 mmol, 66% yield) as a white solid as a mixture ofrotamers in 2:1 ratio; ¹H NMR (300 MHz, DMSO-d₆) δ 8.82 (t, J=5.8 Hz,1H), 8.66 (s, 2H), 8.37-8.23 (m, 1H), 7.99-7.90 (m, 2H), 7.66-6.72 (m,6H), 5.33 and 5.15 (2s, 2H), 4.64-4.51 and 4.28-4.22 (2m, 1H), 4.48 and4.32 (2d, J=5.8 Hz, 2H), 4.17 and 3.84 (2s, 2H), 3.178 and 3.172 (2s,6H), 1.24 and 0.99 (2d, J=6.8 Hz, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.21 and −121.77; MS (ES+): 580.6 (M+1); MS (ES−): 614.6 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(6-fluoro-5-methylpyridin-3-yl)-1H-indole-3-carboxamide(127a)

Reaction of5-bromo-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indole-3-carboxamide(124e) (120 mg, 0.22 mmol) with 6-fluoro-5-methylpyridin-3-ylboronicacid (0.041 g, 0.268 mmol) according the procedure reported in Scheme100 gave after workup and purification by flash column chromatography[silica gel (12 g), eluting with CMA80 in CHCl₃ 0 to30%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(6-fluoro-5-methylpyridin-3-yl)-1H-indole-3-carboxamide(127a) (95 mg, 0.17 mmol, 75% yield) as a white solid as a mixture ofrotamers in 2:1 ratio; ¹H NMR (300 MHz, DMSO-d₆) δ 8.83 (t, J=5.7 Hz,1H), 8.40-8.29 (m, 2H), 8.17-8.08 (m, 1H), 7.98 and 7.97 (2s, 1H),7.61-7.34 (m, 5H), 7.22 and 7.03 (2t, J=7.8 Hz, 1H), 6.94 (bs, 1H), 5.35and 5.18 (2s, 2H), 4.66-4.52 and 4.30-4.22 (2m, 1H), 4.48 and 4.33 (d,J=5.6 Hz, 2H), 4.18 and 3.85 (2s, 2H), 2.34 (s, 3H), 1.24 and 1.00 (d,J=6.8 Hz, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) (a mixture of two rotamers) δ−76.98, −121.21 and −121.78; MS (ES+): 568.6 (M+1), 590.5 (M+23), MS(ES−): 602.5 (M+Cl).

Preparation of2-(3-acetyl-5-(pyridazin-3-ylamino)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(128c) Step-1: Preparation of tert-butyl2-(3-acetyl-5-(pyridazin-3-ylamino)-1H-indol-1-yl)acetate (128a)

Reaction of tert-butyl 2-(3-acetyl-5-bromo-1H-indol-1-yl)acetate (90b)(1.0 g, 2.84 mmol) with pyridazin-3-amine (0.41 g, 4.26 mmol) accordingto the procedure reported in step-1 of Scheme 97 gave after workup andpurification by flash column chromatography [silica gel (40 g), elutingwith CMA80 in CHCl₃ 0 to 20%] tert-butyl2-(3-acetyl-5-(pyridazin-3-ylamino)-1H-indol-1-yl)acetate (128a) (180mg, 0.49 mmol, 17% yield) as light yellow solid; ¹H NMR (300 MHz,DMSO-d₆) δ 9.22 (s, 1H), 8.61 (d, J=4.6 Hz, 1H), 8.45-8.35 (m, 1H), 8.27(s, 1H), 7.73 (dd, J=8.9, 2.1 Hz, 1H), 7.47-7.32 (m, 2H), 7.12-7.02 (m,1H), 5.09 (s, 2H), 2.43 (s, 3H), 1.44 (s, 9H); MS (ES+): 367.5 (M+1);389.5 (M+Na); (ES−): 365.4 (M−1).

Step-2: Preparation of2-(3-acetyl-5-(pyridazin-3-ylamino)-1H-indol-1-yl)acetic acid (128b)

Reaction of tert-butyl2-(3-acetyl-5-(pyridazin-3-ylamino)-1H-indol-1-yl)acetate (128a) (120mg, 0.33 mmol) with TFA (0.63 mL, 8.19 mmol) according to the procedurereported in step-2 of Scheme 2 gave after workup2-(3-acetyl-5-(pyridazin-3-ylamino)-1H-indol-1-yl)acetic acid (128b)(0.12 g, 0.28 mmol, 88% yield) as light orange solid; ¹H NMR (300 MHz,DMSO-d₆) δ 13.45 (brs, 1H), 10.24 (s, 1H), 8.76 (d, J=4.7 Hz, 1H), 8.38(d, J=2.3 Hz, 2H), 7.81 (dd, J=9.3, 4.5 Hz, 1H), 7.62-7.43 (m, 2H),7.32-7.10 (m, 1H), 5.15 (s, 2H), 2.44 (s, 3H); MS (ES+): 311.4 (M+1);(ES−): 309.4 (M−1).

Step-3: Preparation of2-(3-acetyl-5-(pyridazin-3-ylamino)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(128c)

Reaction of 2-(3-acetyl-5-(pyridazin-3-ylamino)-1H-indol-1-yl)aceticacid (128b) (60 mg, 0.19 mmol) withN-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide (19c) (50 mg,0.19 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column [silica gel (12 g),eluting with CMA-80 in CHCl₃ 0-100%]2-(3-acetyl-5-(pyridazin-3-ylamino)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(128c) (54 mg, 0.098 mmol, 51% yield) as an off-white solid as a mixtureof two rotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 9.20 (s, 1H), 8.82 and 8.34(2t, J=5.7 Hz, 1H), 8.65-8.55 (m, 1H), 8.40 (m, 1H), 8.23 and 8.17 (2s,1H), 7.65 (dd, J=8.8, 2.2 Hz, 1H), 7.57-7.34 (m, 4H), 7.27-7.17 (m, 1H),7.12-7.02 (m, 1H), 5.33 and 5.15 (2s, 2H), 4.65-4.53 and 4.31-4.21 (2m,1H), 4.48 and 4.35 (2d, J=5.8 Hz, 2H), 4.19 and 3.86 (2s, 2H), 2.42 and2.41 (2s, 3H), 1.26 and 1.00 (2d, J=6.8 Hz, 6H); ¹⁹F NMR (282 MHz,DMSO-d₆) δ −121.18 and −121.86; MS (ES+): 551.6 (M+1), MS (ES−): 585.5(M+Cl).

Preparation of2-(3-acetyl-5-(3-cyclopropylureido)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(129e) Step-1: Preparation of methyl3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indole-5-carboxylate(129b)

Reaction of 2-(3-acetyl-5-(methoxycarbonyl)-1H-indol-1-yl)acetic acid(129a) (154 mg, 0.56 mmol, prepared according to the procedure reportedby Altmann, Eva et al, in PCT Int. Appl., WO 2012/093101) withN-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide (19c) (174 mg,0.67 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column [silica gel (12 g),eluting with MeOH in CHCl₃ 0-10%] methyl3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indole-5-carboxylate(129b) (261 mg, 0.51 mmol, 90% yield) as a light brown gum; ¹H NMR (300MHz, DMSO-d₆) δ 8.87 (d, J=0.6 Hz) and 8.86 (d, J=0.6 Hz) (2d, 1H), 8.82(t, J=5.7 Hz) and 8.34 (2t, 1H), 8.40 and 8.36 (2s, 1H), 7.85 (dd,J=8.7, 1.7 Hz) and 7.79 (dd, J=8.7, 1.7 Hz) (2dd, 1H), 7.63-6.93 (m,4H), 5.42 and 5.23 (2s, 2H), 4.68-4.51 and 4.28-4.18 (2m, 1H), 4.33 (d,J=6.1 Hz) and 4.25 (d, J=6.3 Hz) (2d, 2H), 4.19 and 3.85 (2s, 2H), 3.884and 3.878 (2s, 3H), 2.47 and 2.45 (2s, 3H), 1.27 (d, J=6.4 Hz) and 1.00(d, J=6.8 Hz) (2d, 6H); ¹⁹F NMR (282 MHz, DMS O-d₆) δ −121.19, −121.76;MS (ES+): 516.5 (M+1), MS (ES−): 514.5 (M−1).

Step-2: Preparation of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indole-5-carboxylicacid (129c)

To a solution of methyl3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indole-5-carboxylate(129b) (560 mg, 1.09 mmol) in THF (8 mL) and MeOH (8 mL) was added asolution of lithium hydroxide hydrate (279 mg, 6.51 mmol) in water (8mL) and stirred at room temperature for 3 days. The reaction mixture wasconcentrated to remove THF and MeOH, diluted with water (4 mL),acidified with 4 N HCl and solid obtained was collected by filtration,dried under vacuum to give3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indole-5-carboxylicacid (129c) (360 mg, 0.72 mmol, 66% yield) as a yellow solid, which wasused in the next step without further purification; ¹H NMR (300 MHz,DMSO-d₆, a mixture of two rotamers) δ 8.88-8.79 and 8.40-8.31 (2m, 3H),7.82 (dd, J=8.6, 1.7 Hz,) and 7.78 (dd, J=8.6, 1.7 Hz) (2dd, 1H),7.62-6.88 (m, 4H), 5.41 and 5.22 (2s, 2H), 4.64-4.51 and 4.29-4.20 (2m,1H), 4.47 (d, J=5.5 Hz) and 4.33 (d, J=6.0 Hz) (2d, 2H), 4.19 and 3.85(2s, 2H), 2.46 and 2.44 (2s, 3H), 1.26 (d, J=6.4 Hz) and 1.00 (d, J=6.8Hz) (2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.19, −121.76; MS (ES+):524.5 & 526.5 (M+Na); MS (ES−): 536.5 & 538.5 (M+Cl).

Step-3: Preparation of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indole-5-carbonylazide (129d)

A suspension of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indole-5-carboxylicacid (129c) (139 mg, 0.28 mmol) in THF (10 mL) was treated withtriethylamine (0.039 μL, 0.28 mmol) and stirred at room temperature for15 min. The mixture was then treated with diphenyl phosphorazidate(0.062 mL, 0.277 mmol) and stirred at room temperature for 15 h. Thereaction mixture was concentrated in vacuum to dryness, solid obtainedwas triturated with DCM, collected by filtration, dried under vacuum toafford3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indole-5-carbonylazide (129d); MS (ES−):

525.5 (M−1)

Step-4: Preparation of2-(3-acetyl-5-(3-cyclopropylureido)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(129e)

A suspension of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indole-5-carbonylazide (129d) (75 mg, 0.14 mmol) in THF/Tol (24 mL, Ratio: 1:2) washeated at reflux for 4h, cooled to room temperature and concentrated invacuum to dryness. The residue obtained was dissolved in THF (20 mL) andACN (10 mL) followed by the addition of cyclopropanamine (16.25 mg, 0.29mmol) and triethylamine (0.060 μL, 0.427 mmol). The reaction mixture wasstirred at room temperature overnight, diluted with EtOAc (100 mL),washed with water (3×), dried, filtered and concentrated in vacuum. Theresidue was purified by column chromatography [silica (12 g), elutingwith CMA80 in CHCl₃ 0 to 40%] followed by preparative HPLC withwater/ACN to give2-(3-acetyl-5-(3-cyclopropylureido)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(129e) (6 mg, 10.79 μma 6% yield) as a white solid after lyophilization;¹H NMR (300 MHz, DMSO-d₆) (a mixture of two rotamers) δ 8.84-8.13 (m,4H), 7.60-6.90 (m, 5H), 6.27 (d, J=2.3 Hz, 1H), 5.29 and 5.11 (2s, 2H),4.66-4.50 and 4.28-4.20 (2m, 1H), 4.47 (d, J=5.4 Hz) and 4.34 (d, J=5.8Hz) (2d, 2H), 4.17 and 3.84 (2s, 2H), 2.40 and 2.39 (2s, 3H), 1.24 (d,J=6.3 Hz) and 1.00 (d, J=6.8 Hz) (2d, 6H), 0.71-0.55 (m, 2H), 0.50-0.31(m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −73.45 (TFA peak), −121.20,−121.82; MS (ES+); 578.5 (M+Na); MS (ES⁻): 554.5 (M−1).

Preparation of2-(3-acetyl-5-(pyridin-2-ylethynyl)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(130a)

Reaction of2-(3-acetyl-5-bromo-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(90d) (301 mg, 0.56 mmol) with 2-ethynylpyridine (58 mg, 0.56 mmol)according to the procedure reported in scheme 92 gave after workup andpurification by flash column chromatography [silica gel 12 g, elutingwith EtOAc/MeOH (9:1) in hexanes 0 to 100%]2-(3-acetyl-5-(pyridin-2-ylethynyl)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(130a) (17 mg, 0.030 mmol, 5% yield) as a dark-yellow solid as a mixtureof two rotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 8.84 (t, J=5.8 Hz, D₂Oexchangeable) and 8.39-8.31 (m) (2H) 8.65-8.57 (m, 1H), 8.43 (d, J=1.5Hz, 1H), 7.92-7.81 (m, 1H), 7.69 and 7.67 (2s, 1H), 7.63-6.94 (m, 6H),5.41 and 5.23 (2s, 2H), 4.65-4.55 and 4.29-4.24 (2m, 1H), 4.52-4.30 (m,2H), 4.19 and 3.86 (2s, 2H), 2.47 and 2.45 (2s, 3H), 1.27 (d, J=6.4 Hz)and 1.01 (d, J=6.7 Hz) (2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.17,−121.76; MS (ES+): 559.5, 561.6 (M+1); MS (ES−): 558.5, 557.5 (M−1),593.5 (M+Cl).

Preparation of2-(3-acetyl-5-(pyridin-3-ylethynyl)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(131a)

Reaction of2-(3-acetyl-5-bromo-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(90d) (301 mg, 0.56 mmol) with 3-ethynylpyridine (58 mg, 0.56 mmol)according to the procedure reported in scheme 92 gave after workup andpurification by flash column chromatography [silica gel 12 g, elutingwith MeOH in CHCl₃ 0 to 20%]2-(3-acetyl-5-(pyridin-3-ylethynyl)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(131a) (14 mg, 0.025 mmol, 5% yield) as a dark-yellow solid as a mixtureof two rotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 8.84 (t, J=5.7 Hz) and8.44-8.32 (t & m, 3H), 8.81-8.78 (m, 1H), 8.60-8.55 (m, 1H), 8.02 (dt,J=7.9, 1.9 Hz, 1H), 7.66-6.94 (m, 6H), 5.41 and 5.22 (2s, 2H), 4.68-4.54and 4.30-4.22 (2m, 1H), 4.48 (d, J=5.6 Hz) and 4.34 (d, J=6.5 Hz) (2d,2H), 4.19 and 3.86 (2s, 2H), 2.46 and 2.45 (2s, 3H), 1.27 (d, J=6.4 Hz)and 1.01 (d, J=6.8 Hz) (2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.18,−121.77; MS (ES+): 559.61, 561.58 (M+1); MS (ES−): 559.5, 557.5 (M−1),593.5 (M+Cl).

Preparation of methyl3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylate(132g) Step-1: Preparation of methyl 3-iodo-1H-indazole-5-carboxylate(132b)

To a solution of methyl 1H-indazole-5-carboxylate (132a) (5 g, 28.4mmol) in THF (40 mL) was added 12 (10.81 g, 42.6 mmol) and KOtBu (7.96g, 71.0 mmol) at 0° C., the resulting mixture was stirred for 3h at roomtemperature. The reaction mixture was diluted with 10% aqueous sodiumthiosulfate and extracted with EtOAc (3×40 mL). The combined organiclayers were washed with water, brine, dried and concentrated in vacuum.The obtained solid was washed with MeOH (20 mL) to give methyl3-iodo-1H-indazole-5-carboxylate (132b) (5.6 g, 18.54 mmol, 65% yield)as a yellow solid; ¹H NMR (300 MHz, DMSO-d₆) δ13.87 (s, 1H), 8.08-8.03(m, 1H), 7.97 (dd, J=8.8, 1.6 Hz, 1H), 7.65 (dd, J=8.8, 0.7 Hz, 1H),3.88 (s, 3H); MS (ES+): 303.2 (M+1); MS (ES−): 301.2 (M−1).

Step-2: Preparation of methyl1-(2-(tert-butoxy)-2-oxoethyl)-3-iodo-1H-indazole-5-carboxylate (132c)

Reaction of methyl 3-iodo-1H-indazole-5-carboxylate (132b) (5 g, 16.55mmol) with tert-butyl 2-bromoacetate (4.84 g, 24.83 mmol) according tothe procedure reported in step-1 of Scheme 56 gave after workup andtrituration of solid with hexane (50 mL) methyl1-(2-tert-butoxy-2-oxoethyl)-3-iodo-1H-indazole-5-carboxylate (132c)(5.74 g, 13.79 mmol, 83% yield) as a yellow solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.16-7.92 (m, 2H), 7.89-7.67 (m, 1H), 5.37 (s, 2H), 3.90 (s,3H), 1.40 (s, 9H); MS (ES+): 439.4 (M+Na).

Step-3: Preparation of methyl1-(2-(tert-butoxy)-2-oxoethyl)-3-cyano-1H-indazole-5-carboxylate (132d)

A mixture of Pd(Ph₃P)₄ (83 mg, 0.072 mmol), methyl1-(2-tert-butoxy-2-oxoethyl)-3-iodo-1H-indazole-5-carboxylate (132c)(300 mg, 0.72 mmol), zinc cyanide (110 mg, 0.94 mmol) in DMF (5 mL) washeated at 120° C. for 30 min on microwave under argon atmosphere. Thereaction was cooled to room temperature diluted with EtOAc (100 mL),washed with water, brine, dried, filtered and concentrated in vacuum.The residue was purified by column chromatography [silica (12 g),eluting with EtOAc in hexane 0 to 30%] to give methyl1-(2-(tert-butoxy)-2-oxoethyl)-3-cyano-1H-indazole-5-carboxylate (132d)(125 mg, 0.4 mmol, 55% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.49 (s, 1H), 8.20-8.10 (m, 1H), 8.07-7.99 (m, 1H), 5.58 (s,2H), 3.92 (s, 3H), 1.41 (s, 9H); MS (ES+): 316.4 (M+1); 338.4 (M+Na); MS(ES−): 314.4 (M−1).

Step-4: Preparation of methyl1-(2-(tert-butoxy)-2-oxoethyl)-3-carbamoyl-1H-indazole-5-carboxylate(132e)

Reaction of methyl1-(2-(tert-butoxy)-2-oxoethyl)-3-cyano-1H-indazole-5-carboxylate (132d)(795 mg, 2.52 mmol) in ethanol (16 mL) using conc. NH₄OH (8 mL, 54.4mmol) and H₂O₂ (aq. 35%, 1.56 mL, 15.13 mmol) according to the procedurereported in Scheme 65 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with DMA80 in DCM 0 to 50%]methyl1-(2-(tert-butoxy)-2-oxoethyl)-3-carbamoyl-1H-indazole-5-carboxylate(132e) (302 mg, 0.91 mmol, 36% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.93-8.83 (m, 1H), 8.03 (dd, J=8.9, 1.6 Hz, 1H), 7.92 (s,1H), 7.89-7.79 (m, 1H), 7.61 (s, 1H), 5.41 (s, 2H), 3.91 (s, 3H), 1.41(s, 9H); MS (ES+): 334.4 (M+1); 356.4 (M+Na); MS (ES−): 332.3 (M−1).

Step-5: Preparation of2-(3-carbamoyl-5-(methoxycarbonyl)-1H-indazol-1-yl)acetic acid (132f)

Reaction of methyl1-(2-(tert-butoxy)-2-oxoethyl)-3-carbamoyl-1H-indazole-5-carboxylate(132e) (3.05 g, 9.15 mmol) with TFA (7.05 mL, 91 mmol) according to theprocedure reported in step-2 of Scheme 2 gave after workup2-(3-carbamoyl-5-(methoxycarbonyl)-1H-indazol-1-yl)acetic acid (132f)(2.7 g, 6.9 mmol, 75% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆)δ 8.93-8.82 (m, 1H), 8.01 (dd, J=8.9, 1.6 Hz, 1H), 7.91 (s, 1H), 7.86(dd, J=8.9, 0.7 Hz, 1H), 7.59 (s, 1H), 5.41 (s, 2H), 3.90 (s, 3H); MS(ES+): 278.3 (M+1).

Step-5: Preparation of methyl3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylate(132g)

Reaction of 2-(3-carbamoyl-5-(methoxycarbonyl)-1H-indazol-1-yl)aceticacid (132f) (100 mg, 0.26 mmol) withN-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide (19c) (66 mg,0.26 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column [silica (12 g),eluting with DMA80 in DCM 0 to 50%] to give methyl3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylate(132g) (62 mg, 0.12 mmol, 47% yield) as an off white solid; ¹H NMR (300MHz, DMSO-d₆) δ 8.91-8.86 (m, 1H), 8.83 (t, J=5.7 Hz) and 8.36 (t, J=5.9Hz) (2t, 1H), 8.06-6.97 (m, 7H), 5.65 and 5.52 (2s, 2H), 4.61-4.49 and4.28-4.21 (2m, 1H), 4.46 (d, J=5.4 Hz) and 4.31 (d, J=5.6 Hz) (2d, 2H),4.18 and 3.84 (2s, 2H), 3.91 and 3.9 (2s, 3H), 1.24 (d, J=6.4 Hz) and0.99 (d, J=6.8 Hz) (2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.22,−121.71; MS (ES+): 518.5 (M+1); MS (ES−): 516.5 (M−1).

Preparation of2-(3-acetyl-5-(methylsulfonamido)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(133c) Step-1: Preparation of tert-butyl2-(3-acetyl-5-(methylsulfonamido)-1H-indol-1-yl)acetate (133a)

To degassed Dioxane (4 mL) in a sealed reactor were added tert-butyl2-(3-acetyl-5-bromo-1H-indol-1-yl)acetate (90b) (500 mg, 1.42 mmol),methanesulfonamide (162 mg, 1.70 mmol), potassium carbonate (392 mg,2.84 mmol), di-tert-butyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine(tBuXphos, 30 mg, 0.071 mmol), Pd₂(dba)₃ (32 mg, 0.035 mmol) and heatedat 90° C. for 16 h. Mixture was cooled to room temperature, filteredover Celite pad and pad was washed with EtOAc (2×10 mL). The combinedfiltrate was washed water (2×30 mL), dried, filtered and concentrated invacuum. The residue obtained was purified by column chromatography[silica gel (24 g), eluting with MeOH-EtOAc (1:9) in hexane 0 to 80%] toafford tert-butyl2-(3-acetyl-5-(methylsulfonamido)-1H-indol-1-yl)acetate (133a) (220 mg,0.6 mmol, 42% yield) as an orange solid; ¹H NMR (300 MHz, DMSO-d₆) δ9.49 (s, 1H), 8.32 (s, 1H), 8.10 (d, J=2.1 Hz, 1H), 7.44 (d, J=8.8 Hz,1H), 7.16 (dd, J=8.8, 2.2 Hz, 1H), 5.10 (s, 2H), 2.88 (s, 3H), 2.42 (s,3H), 1.44 (s, 9H).

Step-2: Preparation of2-(3-acetyl-5-(methylsulfonamido)-1H-indol-1-yl)acetic acid (133b)

Reaction of tert-butyl2-(3-acetyl-5-(methylsulfonamido)-1H-indol-1-yl)acetate (133a) (220 mg,0.6 mmol) with TFA (0.93 mL, 12.01 mmol) according to the procedurereported in step-2 of Scheme 2 gave after workup, trituration of residuewith toluene (2×30 mL) and 30% EtOAc-hexane (10 mL)2-(3-acetyl-5-(methylsulfonamido)-1H-indol-1-yl)acetic acid (133b) (230mg, 0.74 mmol, 90% yield) as light orange solid; ¹H NMR (300 MHz,DMSO-d₆) δ 13.26 (s, 1H D₂O exchangeable), 9.49 (s, 1H), 8.34 (s, 1H),8.10 (d, J=2.1 Hz, 1H), 7.49 (d, J=8.9 Hz, 1H), 7.16 (dd, J=8.8, 2.2 Hz,1H), 5.11 (s, 2H), 2.88 (s, 3H), 2.42 (s, 3H); MS (ES+): 311.3 (M+1), MS(ES−): 309.3 (M−1).

Step-3: Preparation of2-(3-acetyl-5-(methylsulfonamido)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(133c)

Reaction of 2-(3-acetyl-5-(methylsulfonamido)-1H-indol-1-yl)acetic acid(133b) (60 mg, 0.19 mmol) withN-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide (10b) (60 mg,0.23 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column [silica (12 g),eluting with CMA80 in CHCl₃ 0 to 30%]2-(3-acetyl-5-(methylsulfonamido)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(133c) (46 mg, 0.084 mmol, 43% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 9.47 (s, 1H), 8.47 (t, J=5.9 Hz, 1H), 8.29 (s, 1H), 8.10 (d,J=2.1 Hz, 1H), 7.52-7.36 (m, 2H), 7.23 (t, J=7.1 Hz, 1H), 7.17-7.04 (m,2H), 5.42 (s, 2H), 4.35 (d, J=5.7 Hz, 2H), 3.99 (s, 2H), 3.08 (d, J=4.4Hz, 1H), 2.89 (s, 3H), 2.41 (s, 3H), 1.08-0.94 (m, 2H), 0.95-0.82 (m,2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.61; MS (ES+): 549.5 (M+1), MS(ES−): 547.5 (M−1), 583.5 (M+Cl).

Preparation of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-N-(1-phenylethyl)-1H-indole-5-carboxamide(134a)

Reaction of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indole-5-carboxylicacid (129c) (50 mg, 0.1 mmol) with 1-phenylethanamine (20 mg, 0.15 mmol)according to the procedure reported in step-3 of Scheme 2 gave afterworkup and purification by flash column [silica (4 g), eluting with MeOHin CHCl₃ 0 to 10%]3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-N-(1-phenylethyl)-1H-indole-5-carboxamide(134a) (34 mg, 56%) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) (amixture of two rotamers) δ 8.87-8.78 and 8.38-8.27 (2m, 2H), 8.72 (d,J=1.7 Hz) and 8.71 (2d, 1H), 8.35 and 8.30 (2s, 1H), 7.77 (dd, J=8.6,1.8 Hz), and 7.72 (2dd, 1H), 7.56-6.92 (m, 9H), 5.39 and 5.20 (2s, 2H),5.27-5.12 (m, 1H), 4.65-4.51 and 4.29-4.20 2 (m, 1H) 4.48 (d, J=5.5 Hz)and 4.33 (d, J=5.8 Hz) (2d, 2H), 4.19 and 3.85 (2s, 2H), 2.46 and 2.45 2(s, 3H), 1.51 (d, J=3.0 Hz) and 1.49 (d, J=3.1 Hz) (2d, 3H), 1.26 (d,J=6.5 Hz) and 1.00 (d, J=6.8 Hz) (2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.20, −121.79; MS (ES+): 627.6 & 629.6 (M+Na); MS (ES⁻): 639.6 &641.5 (M+Cl).

Preparation of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-N-(pyrimidin-5-yl)-1H-indole-5-carboxamide(135a)

Reaction of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indole-5-carboxylicacid (129c) (50 mg, 0.1 mmol) with pyrimidin-5-amine (14.80 mg, 0.15mmol) according to the procedure reported in step-3 of Scheme 2 gaveafter workup and purification by flash column [silica (4 g), elutingwith MeOH in CHCl₃ 0 to 10%]3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-N-(pyrimidin-5-yl)-1H-indole-5-carboxamide(135a) (31 mg, 54%); ¹H NMR (300 MHz, DMSO-d₆) δ 9.20-9.17 (m, 1H),8.91-8.82 and 8.40-8.33 (2m, 2H), 8.79 (t, J=1.4 Hz) and 8.77 (t, J=1.5Hz) (2t, 1H), 8.55 and 8.52 (2s, 1H), 8.13 (dd, J=8.8, 1.8 Hz) and 8.04(dd, J=8.8, 1.8 Hz) (2dd, 1H), 7.82 (d, J=8.8 Hz) and 7.77 (d, J=8.8 Hz)(2d, 1H), 7.70 (dd, J=4.5, 1.8 Hz) and 7.68 (dd, J=4.5, 1.8 Hz) (2dd,1H), 7.59-6.91 (m, 4H), 5.52 (s) and 5.46-5.17 (m) (2H), 4.67-4.51 and4.30-4.15 (2m, 1H), 4.49 (d, J=5.4 Hz) and 4.34 (d, J=5.7 Hz) (2d, 2H),4.21 and 3.87 (2s, 2H), 1.29 (d, J=6.5 Hz) and 1.01 (d, J=6.7 Hz (2d,6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.18, −121.75.

Preparation of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-N-phenyl-1H-indole-5-carboxamide(136a)

Reaction of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indole-5-carboxylicacid (129c) (50 mg, 0.1 mmol) with aniline (0.014 mL, 0.15 mmol)according to the procedure reported in step-3 of Scheme 2 gave afterworkup and purification by flash column [silica (4 g), eluting with MeOHin CHCl₃ 0 to 10%]3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-N-phenyl-1H-indole-5-carboxamide(136a) (33 mg, 57%) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 10.30and 10.27 (2s, 1H), 8.84 (t, J=5.8 Hz) and 8.35 (2t, 1H), 8.80-8.77 (m,1H), 8.39 and 8.35 (2s, 1H), 7.86-7.77 (m, 3H), 7.60 (d, J=3.7 Hz) and7.57 (d, J=3.7 Hz) (2d, 1H), 7.55-6.97 (m, 6H), 5.42 and 5.24 (2s, 2H),4.65-4.51 and 4.30-4.22 (2m, 1H), 4.49 (d, J=5.6 Hz) and 4.34 (d, J=5.8Hz) (2d, 2H), 4.20 and 3.86 (2s, 2H), 1.27 (d, J=6.4 Hz) and 1.01 (d,J=6.8 Hz) (2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.18, −121.75; MS(ES−): 611.5 & 613.5 (M+Cl).

Preparation of5-bromo-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(137e) Step-1: Preparation of 5-bromo-1H-indazole-3-carboxamide (137b)

To a solution of 5-bromo-1H-indazole-3-carboxylic acid (137a) (3.00 g,12.45 mmol, prepared according to the procedure reported by Hood, Johnand Sunil Kumar in PCT Int. Appl., 2013040215) in DMF (60 mL) was addedammonium chloride (1.997 g, 37.3 mmol), HATU (7.10 g, 18.67 mmol)followed by the drop-wise addition of DIPEA (21.74 mL, 124 mmol). Thereaction mixture was stirred at room temperature for 3 h, quenched withwater (100 mL) and extracted with EtOAc (2×100 mL). The organic layerswere combined washed with brine (50 mL), dried, filtered and evaporatedto dryness. The solid obtained was washed with MeOH (3×10 mL) and driedto afford 5-bromo-1H-indazole-3-carboxamide (137b) (1.33 g, 5.54 mmol,44% yield) as an off-white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 13.77 (s,1H, D₂O exchangeable), 8.31 (dd, J=1.9, 0.8 Hz, 1H), 7.84 (s, 1H),7.64-7.58 (m, 1H), 7.53 (dd, J=8.8, 1.9 Hz, 1H), 7.46 (s, 1H); MS (ES−):240.1, 238.1 (M−2).

Step-2: Preparation of tert-butyl2-(5-bromo-3-carbamoyl-1H-indazol-1-yl)acetate (137c)

Reaction of 5-bromo-1H-indazole-3-carboxamide (137b) (1.2 g, 5.0 mmol)with tert-butyl 2-bromoacetate (0.89 mL, 6.0 mmol) using potassiumcarbonate (1.73 g, 12.5 mmol) as base according to the procedurereported step-1 of Scheme 45 gave after workup tert-butyl2-(5-bromo-3-carbamoyl-1H-indazol-1-yl)acetate (137c) (1.55 g, 4.38mmol, 88% yield) as a light green solid; ¹H NMR (300 MHz, DMSO-d₆) δ8.33 (dd, J=1.9, 0.7 Hz, 1H), 7.84 (s, 1H, D₂O exchangeable), 7.75 (dd,J=9.0, 0.7 Hz, 1H), 7.65-7.59 (m, 1H), 7.53 (s, 1H, D₂O exchangeable),5.37 (s, 2H), 1.41 (s, 9H); MS (ES+): 376.3, 378.3 (M+Na); MS (ES−):354.3, 352.2 (M−2).

Step-3: Preparation of 2-(5-bromo-3-carbamoyl-1H-indazol-1-yl)aceticacid (137d)

Reaction of tert-butyl 2-(5-bromo-3-carbamoyl-1H-indazol-1-yl)acetate(137c) (1.0 g, 2.82 mmol) with TFA (4.35 mL, 56.5 mmol) according to theprocedure reported in step-2 of Scheme 2 gave after workup2-(5-bromo-3-carbamoyl-1H-indazol-1-yl)acetic acid (137d) (806 mg, 2.70mmol, 96% yield) as a yellow solid in the form of TFA adduct; ¹H NMR(300 MHz, DMSO-d₆) δ 13.34 (s, 1H, D₂O exchangeable), 8.33 (d, J=1.8 Hz,1H), 7.84 (s, 1H), 7.78 (d, J=8.9 Hz, 1H), 7.61 (dd, J=9.0, 1.9 Hz, 1H),7.52 (s, 1H), 5.37 (s, 2H); MS (ES+): 298.3, 300.2 (M+2); MS (ES−):595.3, 597.3 (2M−1).

Step-4: Preparation of5-bromo-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(137e)

Reaction of 2-(5-bromo-3-carbamoyl-1H-indazol-1-yl)acetic acid (137d)(100 mg, 0.34 mmol) withN-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide (19c) (104 mg,0.4 mmol) according to the procedure reported in step-3 of Scheme 2 gaveafter workup and purification by flash column chromatography [Silicagel, (24 g) eluting with MeOH in DCM 0-30%),5-bromo-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(137e) (34 mg, 0.063 mmol, 19% yield) as a white solid as a mixture tworotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 8.83 and 8.36 (J=5.7 Hz, 1H) (2t,1H), 8.32 (dd, J=1.8, 0.8 Hz, 1H), 7.82 and 7.79 (2s, 1H), 7.68-6.95 (m,6H), 5.61 and 5.47 (2s, 2H), 4.62-4.48 and 4.28-4.21 (2m, 1H), 4.46 (d,J=5.6 Hz) and 4.31 (d, J=5.9 Hz)(2d, 2H), 4.17 and 3.83 (2s, 2H), 1.23(d, J=6.4 Hz) and 0.98 (d, J=6.8 Hz) (2d, 6H); ¹⁹F NMR (282 MHz,DMSO-d₆) δ −121.22, −121.71; MS (ES+): 538.5 & 540.5 (M+1); MS (ES−):538.4 & 536.4 (M−1).

Preparation of2-(3-acetyl-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(138a)

Reaction of N-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide(10b) (100 mg, 0.39 mmol) with 2-(3-acetyl-1H-indol-1-yl)acetic acid(113a) (85 mg, 0.39 mmol) according to the procedure reported in step-3of Scheme 2 gave after workup and purification by flash columnchromatography [silica gel (24 g), eluting with CMA80 in CHCl₃ 0 to 20%]2-(3-acetyl-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(138a) (115 mg, 0.25 mmol, 65% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.46 (t, J=5.8 Hz, 1H), 8.28 (s, 1H), 8.21-8.14 (m, 1H),7.52-7.40 (m, 2H), 7.28-7.16 (m, 3H), 7.10 (t, J=7.9 Hz, 1H), 5.44 (s,2H), 4.34 (d, J=5.8 Hz, 2H), 3.99 (s, 2H), 3.16-3.02 (m, 1H), 2.43 (s,3H), 1.04-0.96 (m, 2H), 0.96-0.87 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.62; MS (ES+): 456.5 (M+1), 478.5 (M+Na), MS (ES−): 454.4 (M−1),490.4 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indole-3-carboxamide(139d) Step-1: Preparation of tert-butyl2-(3-carbamoyl-1H-indol-1-yl)acetate (139b)

Reaction of 1H-indole-3-carboxamide (139a) (1.0 g, 6.24 mmol) withtert-butyl 2-bromoacetate (1.11 mL, 7.49 mmol) using potassium carbonate(2.16 g, 15.61 mmol) as base according to the procedure reported step-1of Scheme 45 gave after workup tert-butyl2-(3-carbamoyl-1H-indol-1-yl)acetate (139b) (1.55 g, 5.65 mmol, 91%yield) as a yellow white solid; MS (ES+): 275.4 (M+1), 294.7 (M+Na); MS(ES−): 273.3 (M−1)

Step-2: Preparation of 2-(3-carbamoyl-1H-indol-1-yl)acetic acid (139c)

Reaction of tert-butyl 2-(3-carbamoyl-1H-indol-1-yl)acetate (139b) (1.12g, 4.08 mmol) with TFA (6.29 mL, 82 mmol) according to the procedurereported in step-2 of Scheme 2 gave after workup

2-(3-carbamoyl-1H-indol-1-yl)acetic acid (139c) (1.18 g, 3.55 mmol, 87%yield) as a yellow solid in the form of TFA adduct; MS (ES+): 219.3(M+1).

Step-3: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indole-3-carboxamide(139d)

Reaction of 2-(3-carbamoyl-1H-indol-1-yl)acetic acid (139c) (150 mg,0.69 mmol) with N-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide(19c) (213 mg, 0.83 mmol) according to the procedure reported in step-3of Scheme 2 gave after workup and purification by flash columnchromatography [Silica gel, (24 g) eluting with MeOH in DCM 0-30%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indole-3-carboxamide(139d) (43 mg, 0.094 mmol, 14% yield) as a white solid as a mixture tworotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 8.81 (t, J=5.7 Hz) and 8.34 (t,J=5.9 Hz) (2t, 1H), 8.20-8.11 (m, 1H), 7.93 and 7.92 (2s, 1H), 7.59-6.63(m, 8H), 5.30 and 5.13 (2s, 2H), 4.68-4.52 and 4.30-4.23 (2m, 1H), 4.47(d, J=5.6 Hz) and 4.33 (d, J=5.9 Hz) (2d, 2H), 4.17 and 3.84 (2s, 2H),1.23 (d, J=6.5 Hz) and 0.99 (d, J=6.8 Hz) (2d, 6H); ¹⁹F NMR (282 MHz,DMSO-d₆) δ −121.22, −121.81; MS (ES+): 481.5, 483.5 (M+Na), 939.9, 941.9(2M+Na); (ES−): 457.5 (M−1), 493.4, 495.5 (M+Cl).

Preparation of5-bromo-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(140a)

Reaction of N-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide(10b) (517 mg, 2.01 mmol) with2-(5-bromo-3-carbamoyl-1H-indazol-1-yl)acetic acid (137d) (500 mg, 1.68mmol) according to the procedure reported in step-3 of Scheme 2 gaveafter workup and purification by flash column chromatography [silica gel(40 g), eluting with MeOH in DCM 0 to 30%]5-bromo-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(140a) (329 mg, 0.613 mmol, 37% yield) as a light brown solid; ¹H NMR(300 MHz, DMSO-d₆) δ 8.50 (t, J=5.8 Hz, 1H), 8.32 (dd, J=1.9, 0.7 Hz,1H), 7.83 (s, 1H), 7.72-7.64 (m, 1H), 7.56 (dd, J=8.9, 1.9 Hz, 1H),7.52-7.42 (m, 2H), 7.28-7.18 (m, 1H), 7.17-7.06 (m, 1H), 5.68 (s, 2H),4.33 (d, J=5.7 Hz, 2H), 3.98 (s, 2H), 3.13-3.00 (m, 1H), 1.03-0.95 (m,2H), 0.95-0.86 (m, 2H). ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.56; MS (ES+):560.4, 558.4 (M+Na); MS (ES−): 534.3, 536.4 (M−1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(pyrimidin-5-ylamino)-1H-indole-3-carboxamide(141e) Step-1: Preparation of tert-butyl2-(5-bromo-3-cyano-1H-indol-1-yl)acetate (141a)

Reaction of 5-bromo-1H-indole-3-carbonitrile (124a) (2.2 g, 9.95 mmol)with tert-butylbromoacetate (2.06 mL, 13.93 mmol) in acetonitrile (50mL) using potassium carbonate (2.75 g, 19.90 mmol) as base, according tothe procedure reported in step-1 of Scheme 43 gave after workup andpurification by column chromatography [silica gel (40 g), eluting withEtOAc in hexane 0 to 80%] tert-butyl2-(5-bromo-3-cyano-1H-indol-1-yl)acetate (141a) (1.4 g, 4.18 mmol, 42%yield) as an off-white solid; MS (ES+): 335.3, 337.3 (M+2), MS (ES−):369.2, 371.2 (M+Cl).

Step-2: Preparation of2-(3-carbamoyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)acetic acid (141b)

Reaction of tert-butyl 2-(5-bromo-3-cyano-1H-indol-1-yl)acetate (141a)(1.3 g, 3.88 mmol), with pyrimidin-5-amine (369 mg, 3.88 mmol) usingpotassium carbonate (1.07 g, 7.76 mmol),di-tert-butyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine (165 mg,0.389 mmol), Pd₂(dba)₃ (178 mg, 0.19 mmol) according to the procedurereported in step-1 of Scheme 97 gave after workup and purification byflash column chromatography [silica gel (40 g), eluting with MeOH/EtOAc(1:9) in Hexane 0 to 100%]2-(3-carbamoyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)acetic acid (141b)(320 mg, 0.92 mmol, 24% yield) as light colorless foam; ¹H NMR (300 MHz,DMSO-d₆) δ 8.61 (s, 1H), 8.54 (s, 1H), 8.51 (s, 2H), 8.19 (s, 1H), 7.55(d, J=8.8 Hz, 1H), 7.35 (d, J=2.0 Hz, 1H), 7.19 (dd, J=8.8, 2.1 Hz, 1H),5.13 (s, 2H), 1.43 (s, 9H); MS (ES+): 350.4 (M+1), MS (ES−): 348.3(M−1), 384.4 (M+Cl).

Step-3: Preparation of tert-butyl2-(3-carbamoyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)acetate (141c)

Reaction of 2-(3-carbamoyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)aceticacid (141b) (320 mg, 0.92 mmol) in EtOH (10 mL) with conc. NH₄OH (0.71mL, 18.32 mmol) and Hydrogen peroxide (35% aqueous, 0.42 mL, 13.74 mmol)according to the procedure reported in step-1 of Scheme 97 gave afterworkup tert-butyl2-(3-carbamoyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)acetate (141c) (300mg, 0.82 mmol, 89% yield) as an off-white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 10.22 (s, 1H), 8.54 (s, 1H), 8.44 (s, 2H), 7.99 (d, J=2.2 Hz,1H), 7.94 (s, 1H), 7.40 (d, J=8.8 Hz, 1H), 7.06 (dd, J=8.7, 2.2 Hz, 1H),6.85 (brs, 1H), 5.06 (s, 2H), 1.43 (d, J=2.6 Hz, 9H); MS (ES+): 368.5(M+1), 390.5 (M+Na); MS (ES−): 366.4 (M−1), 402.4 (M+Cl).

Step-4: Preparation of2-(3-carbamoyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)acetic acid (141d)

Reaction of tert-butyl2-(3-carbamoyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)acetate (141c) (300mg, 0.82 mmol) with TFA (1.26 mL, 16.33 mmol) according to the procedurereported in step-2 of Scheme 2 gave after workup and trituration ofcrude with toluene (2×30 mL) and 30% EtOAc-hexane (10 mL),2-(3-carbamoyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)acetic acid (141d)(250 mg, 0.8 mmol, 98% yield) as light orange solid; ¹H NMR (300 MHz,DMSO-d₆) δ 13.54 (brs, 1H, D₂O exchangeable) 8.54 (s, 1H), 8.45 (s, 2H),8.00 (d, J=2.2 Hz, 1H), 7.96 (s, 1H), 7.43 (d, J=8.8 Hz, 1H), 7.11-7.01(m, 1H), 5.07 (s, 2H); MS (ES+): 312.4 (M+1); MS (ES−): 310.3 (M−1).

Step-5: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(pyrimidin-5-ylamino)-1H-indole-3-carboxamide(141e)

Reaction of 2-(3-carbamoyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)aceticacid (141d) (70 mg, 0.23 mmol) withN-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide (19c) (64 mg,0.25 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column [silica gel (12 g),eluting with CMA-80 in CHCl₃ 0-50%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(pyrimidin-5-ylamino)-1H-indole-3-carboxamide(141e) (33 mg, 0.06 mmol, 27% yield) as a white solid as a mixture ofrotamers in 2:1; ¹H NMR (300 MHz, DMSO-d₆) δ 8.82 and 8.34 (2t, J=5.9Hz, 1H), 8.531 and 8.538 (2s, 1H), 8.44 (s, 2H), 8.39 (s, 1H), 8.00 and7.99 (2s, 1H), 7.91 (s, 1H), 7.62-6.65 (m, 6H), 5.29 and 5.12 (2s, 2H),4.67-4.52 and 4.30-4.18 (m, 1H), 4.47 and 4.33 (2d, J=5.6 Hz, 2H), 4.16and 3.85 (2s, 2H), 1.23 and 0.99 (2d, J=6.8 Hz, 6H); ¹⁹F NMR (282 MHz,DMSO-d₆) δ −121.20 and −121.77; MS (ES+): 552.6 (M+1), 574.6 (M+Na); MS(ES−): 586.5 (M+Cl).

Preparation of2-(5-amino-7-oxo-6,7-dihydro-2H-pyrazolo[4,3-d]pyrimidin-2-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(142f) Step-1: Preparation of methyl1-(2-(tert-butoxy)-2-oxoethyl)-4-nitro-1H-pyrazole-3-carboxylate (142b)

Reaction of methyl 4-nitro-1H-pyrazole-3-carboxylate (142a) (3 g, 17.53mmol) and tert-butyl 2-bromoacetate (3.11 mL, 21.04 mmol) in DMF (10 mL)using potassium carbonate (3.63 g, 26.3 mmol) according to the procedurereported in step-1 of Scheme 43 gave after workup and purification byflash column chromatography [silica gel eluting with hexanes/EtOAc (1:0to 4:1)] methyl1-(2-(tert-butoxy)-2-oxoethyl)-4-nitro-1H-pyrazole-3-carboxylate (142b)(3.35 g, 67%) as a colorless gum; ¹H NMR (300 MHz, DMSO-d₆) δ 8.98 (s,1H), 5.14 (s, 2H), 3.89 (s, 3H), 1.44 (s, 9H); MS (ES+): 308.3 (M+Na).

Step-2: Preparation of methyl4-amino-1-(2-(tert-butoxy)-2-oxoethyl)-1H-pyrazole-3-carboxylate (142c)

Hydrogenation of methyl1-(2-(tert-butoxy)-2-oxoethyl)-4-nitro-1H-pyrazole-3-carboxylate (142b)(3.19 g, 11.18 mmol) in MeOH (100 mL) using palladium (0.595 g, 0.559mmol) (Pd/C, 10%) as catalyst according to procedure reported in Scheme79 gave after workup4-amino-1-(2-(tert-butoxy)-2-oxoethyl)-1H-pyrazole-3-carboxylate (142c)(2.65 g, 93%) as an off white solid which was used as such in next stepwithout further purification; ¹H NMR (300 MHz, DMSO-d₆) δ 7.17 (s, 1H),4.87 (s, 2H), 4.71 (s, 2H), 3.75 (s, 3H), 1.42 (s, 9H); MS (ES+): 278.4(M+Na).

Step-3: Preparation of2-(5-((methoxycarbonyl)amino)-7-oxo-6,7-dihydro-2H-pyrazolo[4,3-d]pyrimidin-2-yl)aceticacid (142d)

Reaction of methyl4-amino-1-(2-(tert-butoxy)-2-oxoethyl)-1H-pyrazole-3-carboxylate (142c)(530 mg, 2.08 mmol) with(methoxycarbonylamino)(methylthio)methylenecarbamic acid methyl ester(43d) (646 mg) in acetic acid according to the procedure reported instep-2 of Scheme 43 gave after workup and trituration with CHCl₃2-(5-((methoxycarbonyl)amino)-7-oxo-6,7-dihydro-2H-pyrazolo[4,3-d]pyrimidin-2-yl)aceticacid (142d) (223 mg, 40%) as an off-white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 13.35 (bs, 1H), 11.29 (s, 1H), 11.05 (s, 1H), 8.14 (s, 1H),5.18 (s, 2H), 3.74 (s, 3H); MS (ES−): 266.3 (M−1).

Step-4: Preparation of methyl(2-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-7-oxo-6,7-dihydro-2H-pyrazolo[4,3-d]pyrimidin-5-yl)carbamate(142e)

Reaction of2-(5-((methoxycarbonyl)amino)-7-oxo-6,7-dihydro-2H-pyrazolo[4,3-d]pyrimidin-2-yl)aceticacid (142d) (36 mg, 0.14 mmol) withN-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide (19c) (35 mg,0.14 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column [silica gel (12 g),eluting with CHCl₃/MeOH (1:0 to 9:1)] methyl(2-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-7-oxo-6,7-dihydro-2H-pyrazolo[4,3-d]pyrimidin-5-yl)carbamate(142e) (35 mg, 61% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ11.29 (s, 1H), 11.08 (s, 1H), 8.77 (t, J=5.8 Hz) and 8.36 (t, J=5.9 Hz)(2t, 1H), 8.05 and 8.04 (2s, 1H), 7.56-7.08 (m, 3H), 5.44 and 5.27 (2s,2H), 4.64-4.49 and 4.20-4.08 (2m, 1H), 4.42 (d, J=5.6 Hz) and 4.33 (d,J=5.9 Hz) (2d, 2H), 4.12 and 3.84 (2s, 2H), 3.73 (s, 3H), 1.18 (d, J=6.4Hz) and 0.98 (d, J=6.8 Hz) (2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.32, −121.72; MS (ES+): 508.6 (M+1) and 530.5 (M+Na).

Step-5: Preparation of2-(5-amino-7-oxo-6,7-dihydro-2H-pyrazolo[4,3-d]pyrimidin-2-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(142f)

Reaction of methyl(2-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-7-oxo-6,7-dihydro-2H-pyrazolo[4,3-d]pyrimidin-5-yl)carbamate(142e) (32 mg, 0.063 mmol) with 2 N aqueous sodium hydroxide (0.32 mL,0.63 mmol) in MeOH according to the procedure reported in step-4 ofscheme 43 gave after workup and purification by flash column [silica gel(12 g), eluting with CHCl₃/CMA80 (1:0 to 0:1)]2-(5-amino-7-oxo-6,7-dihydro-2H-pyrazolo[4,3-d]pyrimidin-2-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(142f) (6 mg, 32%) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 8.76(t, J=5.8 Hz) & 8.36 (t, J=5.9 Hz) (2t, 1H), 7.67 & 7.63 (2s, 1H),7.55-7.08 (m, 3H), 5.93 (bs, 2H), 5.33 & 5.16 (2s, 2H), 4.41 (d, J=5.6Hz) & 4.34 (d, J=6.0 Hz) (2d, 2H), 4.63-4.52 & 4.19-4.04 (2m, 1H), 4.10& 3.83 (s) (2s, 2H), 1.15 (d, J=6.4 Hz) & 0.98 (d, J=6.8 Hz) (2d, 6H);¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.34, −121.74; MS (ES+): 472.5 (M+Na).

Preparation ofN-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropyl-2-(7-oxo-6,7-dihydro-2H-pyrazolo[4,3-d]pyrimidin-2-yl)acetamide(143f) Step-1: Preparation of methyl1-(2-ethoxy-2-oxoethyl)-4-nitro-1H-pyrazole-3-carboxylate (143a)

Reaction of methyl 4-nitro-1H-pyrazole-3-carboxylate (142a) (1.9 g, 11.1mmol) and 2-bromoacetate (1.508 mL, 13.32 mmol) in DMF (7 mL) usingpotassium carbonate (2.3 g, 16.66 mmol) according to the procedurereported in step-1 of Scheme 43 gave after workup and purification byflash column chromatography [silica gel eluting with hexanes/EtOAc (1:0to 2:1)] methyl1-(2-ethoxy-2-oxoethyl)-4-nitro-1H-pyrazole-3-carboxylate (143a) (2.28g, 80%) as a yellow oil; ¹H NMR (300 MHz, DMSO-d₆) δ 8.99 (s, 1H), 5.26(s, 2H), 4.19 (q, J=7.1 Hz, 2H), 3.89 (s, 3H), 1.22 (t, J=7.1 Hz, 3H);MS (ES+): 258.3 (M+Na).

Step-2: Preparation of methyl4-amino-1-(2-ethoxy-2-oxoethyl)-1H-pyrazole-3-carboxylate (143b)

Hydrogenation of methyl1-(2-ethoxy-2-oxoethyl)-4-nitro-1H-pyrazole-3-carboxylate (143a) (2.19g, 8.5 mmol) in MeOH (80 mL) using palladium (0.45 g, Pd/C, 10%) ascatalyst according to procedure reported in Scheme 79 gave after workupmethyl 4-amino-1-(2-ethoxy-2-oxoethyl)-1H-pyrazole-3-carboxylate (143b)as an off white solid which was used as such in next step withoutfurther purification; MS (ES+): 228.3 (M+Na).

Step-3: Preparation of ethyl2-(7-oxo-6,7-dihydro-2H-pyrazolo[4,3-d]pyrimidin-2-yl)acetate (143d)

A mixture of methyl4-amino-1-(2-ethoxy-2-oxoethyl)-1H-pyrazole-3-carboxylate (143b) (1.75 gof the above crude product from step-2) and formimidamide acetate (143c)(8.08 g, 77 mmol) in ethanol (75 mL) was refluxed for 12 h. The reactionmixture was cooled to room temperature and solid obtained was collectedby filtration, washed with ethanol, and dried under vacuum to give ethyl2-(7-oxo-6,7-dihydro-2H-pyrazolo[4,3-d]pyrimidin-2-yl)acetate (143d)(1.49 g, 82% for two steps) as an off-white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 11.92 (s, 1H), 8.36 (s, 1H), 7.79 (d, J=2.6 Hz, 1H), 5.34 (s,2H), 4.18 (d, J=7.1 Hz, 2H), 1.22 (t, J=7.1 Hz, 3H); MS (ES+): 245.3(M+Na).

Step-4: Preparation of2-(7-oxo-6,7-dihydro-2H-pyrazolo[4,3-d]pyrimidin-2-yl)acetic acid (143e)

Reaction of ethyl2-(7-oxo-6,7-dihydro-2H-pyrazolo[4,3-d]pyrimidin-2-yl)acetate (143d)(200 mg, 0.9 mmol) with 2 N aqueous sodium hydroxide (2.7 mL, 5.4 mmol)in MeOH according to the procedure reported in step-4 of scheme 43 gaveafter workup2-(7-oxo-6,7-dihydro-2H-pyrazolo[4,3-d]pyrimidin-2-yl)acetic acid (143e)(165 mg, 94%) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 13.40 (s,1H), 11.90 (s, 1H), 8.34 (s, 1H), 7.79 (d, J=3.4 Hz, 1H), 5.22 (s, 2H);MS (ES−): 193.1 (M−1),

Step-5: Preparation ofN-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropyl-2-(7-oxo-6,7-dihydro-2H-pyrazolo[4,3-d]pyrimidin-2-yl)acetamide(143f)

Reaction of 2-(7-oxo-6,7-dihydro-2H-pyrazolo[4,3-d]pyrimidin-2-yl)aceticacid (143e) (70 mg, 0.36 mmol) withN-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide (19c) (112 mg,0.43 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column [silica gel (4 g),eluting with CHCl₃/MeOH (1:0 to 9:1)]N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropyl-2-(7-oxo-6,7-dihydro-2H-pyrazolo[4,3-d]pyrimidin-2-yl)acetamide(143f) (85 mg, 54% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ11.86 (bs, 1H), 8.77 (t, J=5.7 Hz) & 8.35 (2t, 1H), 8.25 & 8.24 (2s,1H), 7.78 (t, J=3.1 Hz, 1H), 7.55-7.09 (m, 3H), 5.48 & 5.31 (2s, 2H),4.68-4.48 & 4.22-4.10 (2m, 1H), 4.42 (d, J=5.6 Hz) & 4.33 (d, J=5.7 Hz)(2d, 2H), 4.13 & 3.85 (2s, 2H), 1.19 (d, J=6.4 Hz) & 0.99 (d, J=6.8 Hz)(2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.32, −121.71; MS (ES+): 435.4(M+1).

Preparation of3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (144a)

Reaction of methyl3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylate(132g) (3.2 g, 6.18 mmol) in MeOH/water (50 mL, 5:2, v/v) using NaOH(1.24 g, 30.9 mmol) in water (10 mL), according to the procedurereported in step-4 of scheme 43 gave after workup3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (144a)_(3.04 g, 6.03 mmol, 98% yield) as a white solid; ¹H NMR (300MHz, DMSO-d₆) δ 12.95 (s, 1H), 8.96-8.30 (m, 2H), 7.98 (dd, J=8.9, 1.5Hz) and 7.93 (dd, J=8.9, 1.5 Hz) (2dd, 1H), 7.86 and 7.84 (2s, 1H), 7.69(d, J=9.0 Hz) and 7.61 (d, J=8.9 Hz) (2d, 1H), 7.57-6.92 (m, 4H), 5.64and 5.51 (2s, 2H), 4.63-4.49 and 4.27-4.20 (2m, 1H), 4.46 (d, J=5.4 Hz)and 4.31 (d, J=5.7 Hz) (2d, 2H), 4.18 and 3.83 (2s, 2H), 1.23 (d, J=6.4Hz) and 0.99 (d, J=6.8 Hz) (2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.22, −121.70; MS (ES+): 504.5 (M+1), 526.5 (M+Na); MS (ES−): 502.5(M−1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(3-phenylureido)-1H-indazole-3-carboxamide(145b) Step-1: Preparation of3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (145a)

Reaction of3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (144a) (800 mg, 1.588 mmol) according to the procedure reported instep-3 of Scheme 129 gave after workup3-carbamoyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (145a) (1.32 g, 2.5 mmol), which was used directly in the nextstep without further purification.

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(3-phenylureido)-1H-indazole-3-carboxamide(145b)

Reaction of3-carbamoyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (145a) (112 mg, 0.212 mmol) in toluene (15 mL) with aniline (39.4mg, 0.424 mmol) using TEA (0.059 mL, 0.424 mmol) as base according tothe procedure reported in step-4 of Scheme 129 gave after workup andpurification by column chromatography [silica gel (12 g), eluting withDMA80 in DCM 0 to 40%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(3-phenylureido)-1H-indazole-3-carboxamide(145b) (9 mg, 0.015 mmol, 7% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) (a mixture of two rotamers) δ 8.83 8.77 and 8.42-8.28 (2m, 3H),8.63 (s, 1H), 7.65-6.91 (m, 12H), 5.55 and 5.41 (2s, 2H), 4.62-4.50 and4.30-4.21 (2m, 1H), 4.46 (d, J=4.9 Hz) and 4.32 (d, J=5.2 Hz) (2d, 2H),4.18 and 3.83 (2s, 2H), 1.22 (d, J=6.4 Hz) and 0.99 (d, J=6.7 Hz) (2d,6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.22, −121.74; MS (ES+): 594.6(M+1) MS (ES−): 628.6 (M+Cl).

Preparation of(S)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(4-hydroxybutan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(146b) Step-1: Preparation of(S)—N-(3-chloro-2-fluorobenzyl)-2-((4-hydroxybutan-2-yl)amino)acetamide(146a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (350 mg,1.48 mmol) with (S)-3-aminobutan-1-ol (264 mg, 2.97 mmol) according tothe procedure reported in step-2 of Scheme 35 gave after workup(S)—N-(3-chloro-2-fluorobenzyl)-2-((4-hydroxybutan-2-yl)amino)acetamide(146a) (112, 26%) as a yellow oil, which was used in the next stepwithout further purification; MS (ES+): 289.4 (M+1); MS (ES−): 287.3(M−1).

Step-2: Preparation of(S)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(4-hydroxybutan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(146b)

Reaction of(S)—N-(3-chloro-2-fluorobenzyl)-2-((4-hydroxybutan-2-yl)amino)acetamide(146a) (112 mg, 0.39 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (94 mg, 0.43 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with DMA-80 in DCM 0 to 40%](S)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(4-hydroxybutan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(146b) (40 mg, 0.082 mmol, 21% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.83 (t, J=5.7 Hz) and 8.40 (t, J=5.9 Hz) (2t, 1H), 8.24-8.12(m, 1H), 7.71 (d, J=6.3 Hz, 1H), 7.56-6.99 (m, 7H), 5.83-5.35 (m, 2H),4.95-3.65 (m, 6H), 3.62-3.19 (m, 2H), 1.83-1.38 (m, 2H), 1.25 (d, J=6.5Hz) and 0.98 (d, J=6.8 Hz) (2d, 3H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.25, −121.76; MS (ES+): 490.5 (M+1), 512.5 (M+Na); MS (ES−): 488.5(M−1); [based on NMR, this compound is a mixture of rotamer 1:1 ratio].

Preparation of(1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((3-methyloxetan-3-yl)methyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(147b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-((2-(3-methyloxetan-3-yl)ethyl)amino)acetamide(147a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (292 mg,1.24 mmol) with (3-methyloxetan-3-yl)methanamine (250 mg, 2.47 mmol)according to the procedure reported in step-2 of Scheme 35 gave afterworkup and purification by flash column chromatography [silica (12 g),eluting with EtOAc/MeOH (9:1) in hexane 0 to 60%]N-(3-chloro-2-fluorobenzyl)-2-((2-(3-methyloxetan-3-yl)ethyl)amino)acetamide(147a) (113 mg, 30%) as a colorless oil; MS (ES+): 301.3 (M+1), 323.3(M+Na); MS (ES−): 299.3 (M−1).

Step-2: Preparation of(1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((3-methyloxetan-3-yl)methyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(147b)

Reaction ofN-(3-chloro-2-fluorobenzyl)-2-((2-(3-methyloxetan-3-yl)ethyl)amino)acetamide(147a) (113 mg, 0.38 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (91 mg, 0.4 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with DMA-80 in DCM 0 to 40%](1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((3-methyloxetan-3-yl)methyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(147b) (76 mg, 0.15 mmol, 40% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.83 (t, J=5.6 Hz) and 8.50 (t, J=5.8 Hz) (2t, 1H), 8.19 (d,J=8.1 Hz, 1H), 7.82-7.65 (m, 1H), 7.57-7.10 (m, 7H), 5.54 and 5.49 (2s,2H), 4.54-3.03 (m, 10H), 1.24 and 1.22 (2s, 3H); ¹⁹F NMR (282 MHz,DMSO-d₆) δ −121.16, −121.55; MS (ES+): 524.5 (M+Na); [based on NMR, thiscompound is a mixture of two rotamers 4:1 ratio].

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(3,3-difluoropiperidine-1-carboxamido)-1H-indazole-3-carboxamide(148a)

Reaction of3-carbamoyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (145a) (200 mg, 0.38 mmol) in toluene (15 mL) with3,3-difluoropiperidine hydrochloride (119 mg, 0.756 mmol) using TEA(0.21 mL, 1.51 mmol) as base according to the procedure reported instep-4 of Scheme 129 gave after workup and purification by columnchromatography [silica gel (12 g), eluting with DMA80 in DCM 0 to 40%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(3,3-difluoropiperidine-1-carboxamido)-1H-indazole-3-carboxamide(148a) (36 mg, 0.058 mmol, 15% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) (as a mixture of two rotamers) δ 8.82 (t, J=5.8 Hz) and 8.36(t, J=5.8 Hz) (2t, 1H), 8.78 (s, 1H), 8.19 (s, 1H), 7.71-7.04 (m, 7H),5.54 and 5.41 (2s, 2H), 4.65-4.50 and 4.29-4.21 (2m, 1H), 4.46 (d, J=5.3Hz) and 4.32 (d, J=5.6 Hz) (2d, 2H), 4.21-3.70 (m, 4H), 3.52 (t, 2H),2.17-1.95 (m, 2H), 1.82-1.60 (m, 2H), 1.22 (d, J=6.4 Hz) and 0.99 (d,J=6.8 Hz)(2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −101.17, −121.22,−121.78; MS (ES+): 622.6 (M+1), 644.6 (M+Na); MS (ES−): 620.5 (M−1).

Preparation ofN-(2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)-N-isopropyl-2-(4-oxo-4,5-dihydro-2H-pyrazolo[3,4-d]pyrimidin-2-yl)acetamide(149f) Step-1: Preparation of methyl3-amino-1-(2-ethoxy-2-oxoethyl)-1H-pyrazole-4-carboxylate (149b)

Reaction of methyl 3-amino-1H-pyrazole-4-carboxylate (149a) (4.9 g, 33.0mmol) and 2-bromoacetate (4.48 mL, 39.6 mmol) in DMF (20 mL) usingpotassium carbonate (6.91 g, 49.5 mmol) according to the procedurereported in step-1 of Scheme-43 gave after workup and purification byflash column chromatography [silica gel eluting with hexanes/EtOAc (1:0to 1:1)] methyl5-amino-1-(2-ethoxy-2-oxoethyl)-1H-pyrazole-4-carboxylate (149b) (3.98g, 53%) as a yellow oil; ¹H NMR (300 MHz, DMSO-d₆) δ 7.97 (s, 1H), 5.41(s, 2H), 4.82 (s, 2H), 4.14 (q, J=7.1 Hz, 2H), 3.70 (s, 3H), 1.20 (t,J=7.2 Hz, 3H); MS (ES+): 228.3 (M+1); and methyl5-amino-1-(2-ethoxy-2-oxoethyl)-1H-pyrazole-4-carboxylate (149c) (2.73g, 36%) as a yellow solid; ¹H NMR (300 MHz, DMSO-d₆) δ 7.48 (s, 1H),6.42 (s, 2H), 4.82 (s, 2H), 4.13 (q, J=7.1 Hz, 2H), 3.68 (s, 3H), 1.20(t, J=7.1 Hz, 3H); MS (ES+): 228.3 (M+1).

Step-2: Preparation of ethyl2-(4-oxo-4,5-dihydro-2H-pyrazolo[3,4-d]pyrimidin-2-yl)acetate (149d)

Reaction of methyl3-amino-1-(2-ethoxy-2-oxoethyl)-1H-pyrazole-4-carboxylate (149b) (3.44g, 15.15 mL) with formimidamide acetate (143c) (15.93 g, 151 mmol) inethanol (120 mL) according to the procedure reported in step-3 ofScheme-143 gave after workup and purification by flash columnchromatography [silica gel eluting with CHCl₃/MeOH (1:0 to 9:1)] ethyl2-(4-oxo-4,5-dihydro-2H-pyrazolo[3,4-d]pyrimidin-2-yl)acetate (149d)(979 mg, 29%) as a white solid; %). ¹H NMR (300 MHz, DMSO-d₆) δ 11.80(s, 1H), 8.53 (s, 1H), 7.95 (s, 1H), 5.25 (s, 2H), 4.18 (q, J=7.1 Hz,2H), 1.22 (t, J=7.1 Hz, 3H); MS (ES+): 223.3 (M+1).

Step-3: Preparation of2-(4-oxo-4,5-dihydro-2H-pyrazolo[3,4-d]pyrimidin-2-yl)acetic acid (149e)

Reaction of ethyl2-(4-oxo-4,5-dihydro-2H-pyrazolo[3,4-d]pyrimidin-2-yl)acetate (149d)(200 mg, 0.9 mmol) with 2 N aqueous sodium hydroxide (2.7 mL, 5.4 mmol)in MeOH according to the procedure reported in step-4 of scheme 43 gaveafter workup2-(4-oxo-4,5-dihydro-2H-pyrazolo[3,4-d]pyrimidin-2-yl)acetic acid (149e)(162 mg, 93%) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 13.40 (s,1H), 11.77 (s, 1H), 8.51 (s, 1H), 7.94 (d, J=3.7 Hz, 1H), 5.13 (s, 2H);MS (ES⁻): 193.1 (M−1).

Step-4: Preparation ofN-(2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)-N-isopropyl-2-(4-oxo-4,5-dihydro-2H-pyrazolo[3,4-d]pyrimidin-2-yl)acetamide (149f)

Reaction of 2-(4-oxo-4,5-dihydro-2H-pyrazolo[3,4-d]pyrimidin-2-yl)aceticacid (149e) (70 mg, 0.36 mmol) withN-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide (19c) (112 mg,0.43 mmol) according to the procedure reported in step-3 of Scheme-2gave after workup and purification by flash column [silica gel (4 g),eluting with CHCl₃/MeOH (1:0 to 9:1)]N-(2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)-N-isopropyl-2-(4-oxo-4,5-dihydro-2H-pyrazolo[3,4-d]pyrimidin-2-yl)acetamide(149f) (81 mg, 52% yield) as an off-white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 11.74 (bs, 1H), 8.76 (t, J=5.8 Hz) & 8.36 (t, J=5.9 Hz) (2t,1H) 8.43 & 8.42 (2s, 1H), 7.93 (t, J=2.7 Hz, 1H), 7.54-7.10 (m, 3H),5.40 & 5.23 (2s, 2H), 4.65-4.49 & 4.23-4.10 (2m, 1H), 4.42 (d, J=5.8 Hz)& 4.32 (d, J=5.8 Hz) (2d, 2H), 4.13 & 3.84 (2s, 2H), 1.18 (d, J=6.5 Hz)& 0.98 (d, J=6.8 Hz) (2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.32,−121.71; MS (ES−): 433.5 & 435.3 (M−1); 469.5 & 471.5 (M+Cl).

Preparation ofN5-benzyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-3,5-dicarboxamide(150a)

Reaction of3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (144a) (50 mg, 0.1 mmol) with phenylmethanamine (0.016 mL, 0.149mmol) according to the procedure reported in step-3 of Scheme 2 gaveafter workup and purification by flash column chromatography [silica (4g), eluting with MeOH in DCM (1:0 to 19:1)]N5-benzyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-3,5-dicarboxamide(150a) (25 mg, 43%) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 9.20(t, J=6.0 Hz) and 8.88-8.68 (m) and 8.36 (t, J=5.8 Hz) (3H), 7.98-7.88(m, 1H), 7.81 and 7.79 (2s, 1H), 7.67 (d, J=8.9 Hz) and 7.60 (dd, J=8.9,0.8 Hz) (d & dd, 1H), 7.55-6.96 (m, 9H), 5.63 and 5.49 (2s, 2H),4.60-4.48 and 4.28-4.21 (2m, 3H), 4.46 (d, J=5.7 Hz) and 4.31 (d, J=5.8Hz) (2d, 2H), 4.18 and 3.83 (2s, 2H), 1.23 (d) and 0.99 (d, J=6.8 Hz)(2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.22, −121.73; MS (ES+): 615.6& 617.6 (M+Na); MS (ES−): 627.5 & 629.5 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-N5-phenyl-1H-indazole-3,5-dicarboxamide(151a)

Reaction of3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (144a) (50 mg, 0.1 mmol) with aniline (0.016 mL, 0.18 mmol)according to the procedure reported in step-3 of Scheme 2 gave afterworkup and purification by flash column chromatography [silica (4 g),eluting with MeOH in DCM (1:0 to 19:1)]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-N5-phenyl-1H-indazole-3,5-dicarboxamide(151a) (17 mg, 30%) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 10.44and 10.43 (2s, 1H), 8.89-8.79 (m) and 8.38 (t, J=5.9 Hz) (2H), 8.02-7.92(m, 1H), 7.87-7.77 (m, 3H), 7.75-7.64 (m, 1H), 7.57-6.98 (m, 7H), 5.65and 5.52 2 (s, 2H), 4.61-4.50 and 4.31-4.21 (2m, 1H), 4.47 (d, J=5.5 Hz)and 4.32 (d, J=6.0 Hz (2d, 2H), 4.19 and 3.85 (2s, 2H), 1.24 (d, J=6.2Hz) and 1.00 (d, J=6.8 Hz) (2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.21, −121.70; MS (ES+): 601.6 & 603.6 (M+Na).

Preparation of tert-butyl((cis)-3-(2-(3-carbamoyl-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)acetamido)cyclobutyl)carbamate(152b) Step-1: Preparation of tert-butyl((cis)-3-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)cyclobutyl)carbamate(152a)

Reaction of 2-bromo-N-(3-chloro-2-fluorobenzyl)acetamide (69b) (250 mg,0.89 mmol) with tert-butyl (cis)-3-aminocyclobutylcarbamate (250 mg,1.34 mmol) according to the procedure reported in step-2 of Scheme 35gave after workup and purification by flash column chromatography[silica gel 12 g, eluting with MeOH in DCM 0 to 50%] tert-butyl((cis)-3-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)cyclobutyl)carbamate(152a) (243 mg, 0.63 mmol, 71% yield) as a thick yellow oil. MS (ES+):386.5 (M+1); MS (ES−): 384.4 (M−1).

Step-2: Preparation of tert-butyl((cis)-3-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)cyclobutyl)carbamate(152a)

Reaction of tert-butyl((cis)-3-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)cyclobutyl)carbamate(152a) (114 mg, 0.3 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (78 mg, 0.36 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [Silica gel, (12 g) eluting with MeOH in DCM from 0-20%]tert-butyl((cis)-3-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)cyclobutyl)carbamate(152a) (122 mg, 0.21 mmol, 70% yield) as a white solid as a mixture tworotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 8.80 and 8.40 (2t, J=5.9 Hz, 1H),8.20-8.15 (m, 1H), 7.69 (bs, 1H), 7.59 and 7.57 (2s, 1H), 7.53-6.99 (m,6H), 5.56 and 5.36 (2s, 2H), 4.47 (d, J=5.6 Hz) and 4.37-4.25 (m) and4.04 (s) (5H), 3.82-3.55 (m, 1H), 2.60-2.53 and 2.36-1.82 (2m, 4H), 1.38and 1.37 (2s, 9H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.25, −121.60. MS(ES−): 621.5, 623.5 (M+Cl).

Preparation of1-(2-(((cis)-3-aminocyclobutyl)(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(153a)

Reaction of tert-butyl((cis)-3-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)cyclobutyl)carbamate(152a) (109 mg, 0.19 mmol) with TFA (0.286 mL, 3.71 mmol) according tothe procedure reported in step-2 of Scheme 2 gave after workup andpurification by flash column chromatography [Silica gel, (8 g) elutingwith DMA80 in DCM 0-30%)]1-(2-(((cis)-3-aminocyclobutyl)(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(153a) (15 mg, 0.031 mmol, 17% yield) as a white solid as a mixture oftwo rotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 8.96-8.89 and 8.41 (t, J=6.0Hz), (m & t, 1H, D₂O exchangeable), 8.21-8.13 (m, 1H), 7.68 (s, 1H, D₂Oexchangeable), 7.61-7.00 (m, 7H), 5.53 and 5.40 (2s, 2H), 4.47 (d, J=5.6Hz) and 4.38-3.97 (m) (5H), 3.03-2.85 (m, 1H), 2.32-1.47 (m, 4H); ¹⁹FNMR (282 MHz, DMSO-d₆) δ −121.23, −121.62; MS (ES+): 487.5 (M+1); MS(ES−): 485.5 (M−1), 521.4, 523.4 (M+Cl).

Preparation ofN-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropyl-2-(3-(2,2,2-trifluoroacetyl)-1H-indol-1-yl)acetamide(154d) Step-1: Preparation of tert-butyl2-(3-(2,2,2-trifluoroacetyl)-1H-indol-1-yl)acetate (154b)

Reaction of 2,2,2-trifluoro-1-(1H-indol-3-yl)ethanone (154a) (800 mg,3.75 mmol) with tert-butyl 2-bromoacetate (1.46 g, 7.51 mmol) usingPotassium carbonate (1.03 g, 7.51 mmol) as base in acetonitrile (50 mL)according to the procedure reported step-1 of Scheme 43 gave afterworkup and purification by flash column chromatography [silica gel (24g), eluting with EtOAc-hexane 0 to 60%] tert-butyl2-(3-(2,2,2-trifluoroacetyl)-1H-indol-1-yl)acetate (154b) (1.15 g, 3.51mmol, 94% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 8.60 (q,J=1.9 Hz, 1H), 8.23-8.17 (m, 1H), 7.63-7.57 (m, 1H), 7.44-7.35 (m, 2H),5.27 (s, 2H), 1.43 (s, 9H); MS (ES+) 328.4 (M+1), MS (ES−): 326.4,(M−1), 362.3 (M+Cl).

Step-2: Preparation of 2-(3-(2,2,2-trifluoroacetyl)-1H-indol-1-yl)aceticacid (154c)

Reaction of tert-butyl2-(3-(2,2,2-trifluoroacetyl)-1H-indol-1-yl)acetate (154b) (1.1 g, 3.36mmol) with TFA (3.88 mL, 50.4 mmol) according to the procedure reportedin step-2 of Scheme 2 gave after workup and trituration of crude productwith 30% EtOAc-hexane (10 mL)2-(3-(2,2,2-trifluoroacetyl)-1H-indol-1-yl)acetic acid (154c) (650 mg,2.4 mmol, 71% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 13.38(s, 1H, D₂O exchangeable), 8.64-8.55 (m, 1H), 8.26-8.14 (m, 1H),7.70-7.58 (m, 1H), 7.44-7.30 (m, 2H), 5.28 (s, 2H); MS (ES+) 272.3(M+1), 294.3 (M+Na), MS (ES−); 270.2, (M−1).

Step-3: Preparation ofN-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropyl-2-(3-(2,2,2-trifluoroacetyl)-1H-indol-1-yl)acetamide(154d)

Reaction of 2-(3-(2,2,2-trifluoroacetyl)-1H-indol-1-yl)acetic acid(154c) (80 mg, 0.3 mmol) withN-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide (19c) (76 mg,0.3 mmol) according to the procedure reported in step-3 of Scheme 2 gaveafter workup and purification by flash column chromatography [silica gel(12 g), eluting with DMA80-DCM 0 to 20%]N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropyl-2-(3-(2,2,2-trifluoroacetyl)-1H-indol-1-yl)acetamide(154d) (115 mg, 0.23 mmol, 76% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) (a mixture of two rotamers) δ 8.83 and 8.34 (2t, J=5.7 Hz, 1H),8.56 and 8.47 (2d, J=2.0 Hz, 1H), 8.23-8.17 (m, 1H), 7.67-6.92 (m, 6H),5.51 and 5.30 (2s, 2H), 4.64-4.54 and 4.29-4.19 (2m, 1H), 4.48 and 4.33(2d, J=5.6 Hz, 2H), 4.18 and 3.85 (2s, 2H), 1.27 and 1.00 (2d, J=6.8 Hz,6H); ¹⁹F NMR (282 MHz, DMSO-d₆) (a mixture of two rotamers) δ −71.30 and−71.33, −121.19 and −121.86; MS (ES+) 512.5 (M+1), 534.5 (M+Na), MS(ES−): 510.5 (M−1), 546.5 (M+Cl).

Preparation of2-(3-acetyl-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(155d) Step-1: Preparation of tert-butyl2-(3-acetyl-1H-indazol-1-yl)acetate (155b)

Reaction of 1-(1H-indazol-3-yl)ethanone (155a) (800 mg, 5.0 mmol) withtert-butyl 2-bromoacetate (1.47 g, 10 mmol) using Potassium carbonate(1.38 g, 10 mmol) as base in acetonitrile (50 mL) according to theprocedure reported step-1 of Scheme 43 gave after workup andpurification by flash column chromatography [silica gel (24 g), elutingwith EtOAC-hexane 0 to 60%] tert-butyl2-(3-acetyl-1H-indazol-1-yl)acetate (155b) (1.3 g, 4.74 mmol, 95% yield)as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 8.19 (dt, J=8.1, 1.0 Hz,1H), 7.75 (dt, J=8.5, 0.9 Hz, 1H), 7.51 (ddd, J=8.4, 6.9, 1.2 Hz, 1H),7.36 (ddd, J=7.9, 6.9, 0.9 Hz, 1H), 5.45 (s, 2H), 2.62 (s, 3H), 1.42 (s,9H); MS (ES+) 297.4 (M+Na); MS (ES−): 273.4 (M−1).

Step-2: Preparation of 2-(3-acetyl-1H-indazol-1-yl)acetic acid (155c)

Reaction of tert-butyl 2-(3-acetyl-1H-indazol-1-yl)acetate (155b) (1 g,3.65 mmol) with TFA (5.62 mL, 72.9 mmol) according to the procedurereported in step-2 of Scheme 2 gave after workup and trituration ofcrude product with 30% EtOAc-hexane (10 mL)2-(3-acetyl-1H-indazol-1-yl)acetic acid (155c) (800 mg, 3.67 mmol, 101%yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 13.35 (s, 1H), 8.19(dt, J=8.1, 1.0 Hz, 1H), 7.79 (dt, J=8.5, 0.9 Hz, 1H), 7.50 (ddd, J=8.4,6.9, 1.2 Hz, 1H), 7.36 (ddd, J=8.0, 6.9, 0.9 Hz, 1H), 5.46 (s, 2H), 2.62(s, 3H); MS (ES+) 219.3 (M+1), 241.3 (M+Na), MS (ES−): 217.2 (M−1).

Step-3: Preparation of2-(3-acetyl-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(155d)

Reaction of 2-(3-acetyl-1H-indazol-1-yl)acetic acid (155c) (65 mg, 0.3mmol) with N-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide (19c)(77 mg, 0.3 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup and purification by flash columnchromatography [silica gel (12 g), eluting with DMA80-DCM; 0 to 20%]2-(3-acetyl-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(155d) (120 mg, 0.26 mmol, 88% yield) as a white solid as a mixture oftwo rotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 8.83 and 8.34 (t, J=5.7 Hz)(2t, 1H), 8.21-8.16 (m, 1H), 7.72-6.96 (m, 6H), 5.70 and 5.53 (2s, 2H),4.62-4.50 and 4.32-4.19 (2m, 1H), 4.47 and 4.32 (2d, J=5.6 Hz, 2H), 4.18and 3.84 (s, 2H), 2.69 and 2.61 (2s, 3H), 1.25 and 1.00 (d, J=6.8 Hz,6H). ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.21, −121.76; MS (ES+) 458.4,459.5 (M+1), 481.5 (M+Na), MS (ES−): 493.4 (M+Cl).

Preparation of2-(3-acetyl-5-bromo-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(156f) Step-1: Preparation of5-bromo-N-methoxy-N-methyl-1H-indazole-3-carboxamide (156b)

To a solution of 5-bromo-1H-indazole-3-carboxylic acid (156a) (1 g, 4.15mmol) in DMF (20 mL) was added CDI (0.81 g, 4.98 mmol) and stirred at65° C. for 15 min. The resultant clear solution was cooled to RT, addedN,O-dimethylhydroxylamine hydrochloride (0.49 g, 5 mmol) and continuedstirring at 65° C. for 3h. Mixture was cooled to RT, concentrated undervacuum and resultant solution was diluted with water (100 mL) andstirred for 10 min. The solid obtained was collected by filtration,washed with water (3×5 mL) and dried to afford5-bromo-N-methoxy-N-methyl-1H-indazole-3-carboxamide (156b) (830 mg,2.92 mmol, 70% yield) as an off-white solid; ¹H NMR (300 MHz, DMSO-d₆) δ13.85 (s, 1H), 8.18 (d, J=1.8 Hz, 1H), 7.69-7.49 (m, 2H), 3.78 (s, 3H),3.45 (s, 3H); MS (ES+) 284.3, 286.2 (M+2), 306.3, 308.3 (M+Na); MS(ES−): 318.2, 320.2 (M+Cl).

Step-2: Preparation of 1-(5-bromo-1H-indazol-3-yl)ethanone (156c)

To a solution of 5-bromo-N-methoxy-N-methyl-1H-indazole-3-carboxamide(156b) (820 mg, 2.89 mmol) in THF (30 mL) at 0° C. under argonatmosphere was added MeLi (8.66 mL, 8.66 mmol). The mixture was slowlywarmed to RT and continued to stir for 3h at RT. Mixture was poured into1 N aqueous KHSO₄ solution (50 mL) and then diluted with EtOAc (40 mL).Layers were separated, aqueous layer was extracted with EtOAc (1×40 mL)and the combined organics were washed with brine, dried, filtered andconcentrated to afford crude product as a dark green solid. This solidwas suspended in 30% EtOAc-hexane (10 mL) and sonicated for few minutes.The solid obtained was collected by filtration, washed with 30%EtOAc-hexane (2×2 mL) to afford 1-(5-bromo-1H-indazol-3-yl)ethanone(156c) (470 mg, 1.97 mmol, 68% yield) as light green solid; ¹H NMR (300MHz, DMSO-d₆) δ 14.06 (s, 1H), 8.30 (dd, J=1.8, 0.8 Hz, 1H), 7.68 (dd,J=8.8, 0.7 Hz, 1H), 7.58 (dd, J=8.9, 1.9 Hz, 1H), 2.63 (s, 3H); MS (ES+)239.2, 241.2 (M+2), MS (ES−): 237.1, 239.1 (M−2), 273.2, 275.1 (M+Cl).

Step-3: Preparation of tert-butyl2-(3-acetyl-5-bromo-1H-indazol-1-yl)acetate (156d)

Reaction of 1-(5-bromo-1H-indazol-3-yl)ethanone (156c) (400 mg, 1.67mmol) with tert-butyl 2-bromoacetate (0.49 mL, 3.35 mmol) usingPotassium carbonate (0.46 g, 3.35 mmol) as base in acetonitrile (20 mL)according to the procedure reported step-1 of Scheme 43 gave afterworkup and purification by flash column chromatography [silica gel (12g), eluting with EtOAc-hexane 0 to 100%] tert-butyl2-(3-acetyl-5-bromo-1H-indazol-1-yl)acetate (156d) (480 mg, 1.36 mmol,81% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 8.32 (dd,J=1.9, 0.7 Hz, 1H), 7.79 (dd, J=9.0, 0.7 Hz, 1H), 7.67 (dd, J=8.9, 1.9Hz, 1H), 5.48 (s, 2H), 2.62 (s, 3H), 1.42 (s, 9H); MS (ES+): 375.3,377.3 (M+2), MS (ES−): 387.3, 389.3 (M+Cl).

Step-4: Preparation of 2-(3-acetyl-5-bromo-1H-indazol-1-yl)acetic acid(156e)

Reaction of tert-butyl 2-(3-acetyl-5-bromo-1H-indazol-1-yl)acetate(156d) (480 mg, 1.36 mmol) with TFA (2.09 mL, 27.2 mmol) according tothe procedure reported in step-2 of Scheme 2 gave after workup andtrituration of crude product with 20% EtOAc-hexane (10 mL)2-(3-acetyl-5-bromo-1H-indazol-1-yl)acetic acid (156e) (400 mg, 1.35mmol, 99% yield) as an off-white solid; ¹H NMR (300 MHz, DMSO-d₆) δ13.42 (s, 1H), 8.32 (d, J=1.9, 0.7 Hz, 1H), 7.82 (dd, J=9.0, 0.7 Hz,1H), 7.66 (dd, J=9.0, 1.9 Hz, 1H), 5.48 (s, 2H), 2.62 (s, 3H); MS (ES+):297.2, 299.2 (M+2), 319.2, 321.2 (M+Na); MS (ES−): 295.2, 297.2 (M−2).

Step-5: Preparation of2-(3-acetyl-5-bromo-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(156f)

Reaction of 2-(3-acetyl-5-bromo-1H-indazol-1-yl)acetic acid (156e) (70mg, 0.24 mmol) withN-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide (19c) (61 mg,0.24 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column chromatography[silica gel (12 g), eluting with DMA80-DCM; 0 to 20%]2-(3-acetyl-5-bromo-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(156f) (93 mg, 0.173 mmol, 73% yield) as a white solid as a mixture oftwo rotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 8.83 and 8.34 (2t, J=5.7 Hz,1H), 8.32-8.30 (m, 1H), 7.74-6.91 (m, 5H), 5.72 and 5.55 (2s, 2H),4.62-4.50 and 4.30-4.19 (2m, 1H), 4.46 and 4.31 (2d, J=5.6 Hz, 2H), 4.17and 3.84 (2s, 2H), 2.69 and 2.61 (2s, 3H), 1.24 and 0.99 (2d, J=6.8 Hz,6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.22, −121.72; MS(ES−) 535.4, 537.4(M−2), 571.4, 573.4; (M+Cl).

Preparation of2-(3-(1-acetyl-1H-indol-3-yl)-1-isopropylureido)-N-(3-chloro-2-fluorobenzyl)acetamide(157c) Step-1: Preparation of 1-acetyl-1H-indole-3-carboxylic acid(157b)

To a solution of 1H-indole-3-carboxylic acid (157a) (10 g, 62.1 mmol),TEA (19.03 mL, 137 mmol) and DMAP (1.516 g, 12.41 mmol) in DCM (100 mL)cooled to 0° C. was added drop-wise acetyl chloride (4.41 mL, 62.1 mmol)and stirred for 3h at RT. The reaction mixture was poured into anaqueous 1 N HCl solution, the solid obtained was collected byfiltration, washed with water, MeOH and dried to give1-acetyl-1H-indole-3-carboxylic acid (157b) (10.2 g, 50.2 mmol, 81%yield) as an off white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 12.83 (s, 1H),8.44 (s, 1H), 8.39-8.31 (m, 1H), 8.13-8.05 (m, 1H), 7.43-7.32 (m, 2H),2.74 (s, 3H); MS (ES+): 204.2 (M+1); (ES−) 202.2 (M−1).

Step-2: Preparation of2-(3-(1-acetyl-1H-indol-3-yl)-1-isopropylureido)-N-(3-chloro-2-fluorobenzyl)acetamide(157c)

To a solution of 1-acetyl-1H-indole-3-carboxylic acid (157b) (0.1 g,0.49 mmol) in dioxane (10 mL) was added triethylamine (0.2 mL, 1.4mmol), diphenylphospharyl azide (0.21 mL, 0.984 mmol) and stirred at RTfor 2 h. To the mixture addedN-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide (19c) (127 mg,0.49 mmol) and mixture was heated at 90° C. for 4h. Mixture was cooledto RT, partitioned between saturated aqueous NaHCO₃ (60 mL) and EtOAc(60 mL). Layers were separated and aqueous layer was extracted withEtOAc (50 mL). The combined organics were washed with brine, dried,filtered, concentrated in vacuum and the residue obtained was purifiedby flash column chromatography [silica gel, (12 g) eluting with EtOAc inhexanes 0 to 100%] to afford2-(3-(1-acetyl-1H-indol-3-yl)-1-isopropylureido)-N-(3-chloro-2-fluorobenzyl)acetamide(157c) (95 mg, 0.21 mmol, 42% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 9.10 (s, 1H), 8.78 (t, J=5.8 Hz, 1H), 8.33 (d, J=8.1 Hz, 1H),7.84 (s, 1H), 7.70 (d, J=7.6 Hz, 1H), 7.54-7.44 (m, 1H), 7.42-7.23 (m,3H), 7.18-7.10 (m, 1H), 4.56-4.34 (m, 3H), 3.98 (s, 2H), 2.58 (s, 3H),1.10 (d, J=6.7 Hz, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.32; MS (ES+):459.5 (M+1), 481.5 (M+Na); MS (ES−): 457.5 (M−1), 493.4 (M+Cl).

Preparation of2-(3-acetyl-5-bromo-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(158a)

Reaction of N-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide(10b) (332 mg, 1.29 mmol) with2-(3-acetyl-5-bromo-1H-indazol-1-yl)acetic acid (156e) (320 mg, 1.06mmol) according to the procedure reported in step-3 of Scheme 2 gaveafter workup and purification by [silica (12 g), eluting with DMA80 inDCM from 0 to 20%]2-(3-acetyl-5-bromo-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(158a) (0.48 g, 0.9 mmol, 83% yield) as a colorless foam; ¹H NMR (300MHz, DMSO-d₆) δ 8.48 (t, J=5.9 Hz, 1H), 8.31 (dd, J=1.8, 0.7 Hz, 1H),7.73 (dd, J=9.0, 0.7 Hz, 1H), 7.60 (dd, J=8.9, 1.9 Hz, 1H), 7.51-7.41(m, 1H), 7.26-7.18 (m, 1H), 7.14-7.05 (m, 1H), 5.77 (s, 2H), 4.33 (d,J=5.8 Hz, 2H), 3.98 (s, 2H), 3.18-3.02 (m, 1H), 2.62 (s, 3H), 1.09-0.95(m, 2H), 0.95-0.79 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.57; MS(ES+): 535.4 (M+1), 557.5 (M+Na), MS (ES−): 533.4 (M−1), 569.4 (M+Cl).

Preparation of2-(3-acetyl-5-(2-(dimethylamino)pyrimidin-5-yl)-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(159a)

Reaction of2-(3-acetyl-5-bromo-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(158a) (125 mg, 0.23 mmol) with 2-(dimethylamino)pyrimidin-5-ylboronicacid (0.047 g, 0.280 mmol) according the procedure reported in Scheme100 gave after workup and purification by flash column chromatography[silica gel (12 g), eluting with CMA80 in CHCl₃ 0 to 20%]2-(3-acetyl-5-(2-(dimethylamino)pyrimidin-5-yl)-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(159a) (93 mg, 0.16 mmol, 69% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.71 (s, 2H), 8.48 (t, J=5.9 Hz, 1H), 8.29 (dd, J=1.7, 0.9Hz, 1H), 7.79 (dd, J=8.8, 0.9 Hz, 1H), 7.72 (dd, J=8.8, 1.7 Hz, 1H),7.50-7.41 (m, 1H), 7.28-7.18 (m, 1H), 7.15-7.06 (m, 1H), 5.78 (s, 2H),4.34 (d, J=5.7 Hz, 2H), 4.00 (s, 2H), 3.19 (s, 6H), 3.16-3.08 (m, 1H),2.63 (s, 3H), 1.09-0.99 (m, 2H), 0.96-0.88 (m, 2H); ¹⁹F NMR (282 MHz,DMSO-d₆) δ −121.58; MS (ES+): 578.7 (M+1), 600.6 (M+Na); MS (ES−) 576.5(M−1), 612.5 (M+Cl).

Preparation of2-(3-acetyl-5-(pyrimidin-5-yl)-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(160a)

Reaction of2-(3-acetyl-5-bromo-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(158a) (125 mg, 0.23 mmol) with pyrimidin-5-ylboronic acid (0.035 g,0.280 mmol) according the procedure reported in Scheme 100 gave afterworkup and purification by flash column chromatography [silica gel (12g), eluting with CMA80 in CHCl₃ 0 to 20%]2-(3-acetyl-5-(pyrimidin-5-yl)-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(160a) (96 mg, 0.18 mmol, 77% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 9.22 (s, 1H), 9.19 (s, 2H), 8.52-8.43 (m, 2H), 7.89 (bs, 2H),7.51-7.39 (m, 1H), 7.29-7.18 (m, 1H), 7.16-7.06 (m, 1H), 5.82 (s, 2H),4.35 (d, J=5.8 Hz, 2H), 4.00 (s, 2H), 3.20-3.09 (m, 1H), 2.66 (s, 3H),1.10-1.00 (m, 2H), 0.97-0.88 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.58; MS (ES+): 535.6 (M+1), 557.6 (M+Na); MS (ES−): 569.5 (M+Cl).

Preparation of1-(2-((((trans)-3-aminocyclobutyl)methyl)(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(161c) Step-1: Preparation of tert-butyl(trans-3-(((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)methyl)cyclobutyl)carbamate(161a)

Reaction of 2-bromo-N-(3-chloro-2-fluorobenzyl)acetamide (69b) (250 mg,0.89 mmol) tert-butyl (trans)-3-(aminomethyl)cyclobutylcarbamate (268mg, 1.34 mmol) according to the procedure reported in step-2 of Scheme35 gave after workup and purification by flash column chromatography[silica gel 12 g, eluting with MeOH in DCM 0 to 20%] tert-butyl((trans)-3-(((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)methyl)cyclobutyl)carbamate(161a) (152 mg, 0.38 mmol, 43% yield) as a white solid; MS (ES+): 400.5(M+1), 799.8 (2M+1), 422.5 (M+Na); MS (ES−): 434.5 (M+Cl).

Step-2: Preparation of tert-butyl((trans)-3-((2-(3-carbamoyl-1H-indazol-1-yl)-N-(2-((3-(161b)

Reaction tert-butyl((trans)-3-(((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)methyl)cyclobutyl)carbamate(161a) (85 mg, 0.21 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (56 mg, 0.26 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [Silica gel, (24 g) eluting with MeOH in CHCl₃ 0-10%]tert-butyl((trans)-3-((2-(3-carbamoyl-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)acetamido)methyl)cyclobutyl)carbamate(161b) (59 mg, 0.1 mmol, 46% yield) as a white solid as a mixture tworotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 8.81 & 8.48 (t, J=5.6 Hz) (2t,1H), 8.19 & 8.17 (2s, 1H), 7.73 (bs, 1H), 7.64-7.00 (m, 7H), 5.59 & 5.46(s, 2H), 4.46 (d, J=5.6 Hz) & 4.32 (d, J=5.8 Hz) (2d, 2H), 4.29-3.88 (m,3H), 3.62 (d, J=7.7 Hz, 1H), 2.27 (s, 1H), 2.05 (t, J=7.0 Hz, 1H),1.97-1.75 (m, 3H), 1.38 & 1.35 (2s, 9H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.30, −121.67; MS (ES+): 601.7 (M+1), 623.7, 625.7 (M+Na); MS (ES−):600.6 (M−1), 635.7, 637.6 (M+Cl).

Step-3: Preparation of1-(2-((((trans)-3-aminocyclobutyl)methyl)(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(161c)

Reaction of tert-butyl((trans)-3-((2-(3-carbamoyl-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)acetamido)methyl)cyclobutyl)carbamate(161b) (56 mg, 0.09 mmol) with TFA (0.144 mL, 1.863 mmol) according tothe procedure reported in step-2 of Scheme 2 gave after workup andpurification by flash column chromatography [Silica gel, (8 g) elutingwith CMA50 in DCM 0-100%)1-(2-((((trans)-3-aminocyclobutyl)methyl)(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(161c) (24 mg, 0.048 mmol, 51% yield) as an off-white solid; ¹H NMR (300MHz, DMSO-d₆) δ 8.81 (t, J=5.7 Hz) and 8.45 (t, J=5.8 Hz) (2t, 1H),8.21-8.15 (m, 1H), 7.73 (s, 1H), 7.60-7.00 (m, 7H), 5.57 and 5.47 (2s,2H), 4.45 (d, J=5.5 Hz) and 4.32 (d, J=5.7 Hz) (2d, 2H), 4.22 and 3.93(2s, 2H), 2.36-1.44 (m, 5H); ¹H NMR (300 MHz, DMSO-d₆, D₂O exchange) δ8.22-8.14 (m, 1H), 7.61-7.01 (m, 7H), 5.59 & 5.45 (2s, 2H), 4.46 and4.34 and 4.23 (3s, 3H), 3.67-3.20 (m, 3H), 2.40-1.56 (m, 5H); ¹⁹F NMR(282 MHz, DMSO-d₆) δ −121.24, −121.64; MS (ES+): 501.6 (M+1), 523.6(M+Na); MS (ES−): 499.5 (M−1), 535.5 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(3-cyclopropylureido)-1H-indazole-3-carboxamide(162a)

Reaction of3-carbamoyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (145a) (270 mg, 0.51 mmol) in toluene (15 mL) withcyclopropanamine (58.3 mg, 1.02 mmol) using TEA (0.29 mL, 2.04 mmol) asbase according to the procedure reported in step-4 of Scheme 129 gaveafter workup and purification by column chromatography [silica gel (12g), eluting with DMA80 in DCM 0 to 40%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(3-cyclopropylureido)-1H-indazole-3-carboxamide(162a) (29 mg, 0.052 mmol, 11% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) (a mixture of two rotamers) δ 8.82 (t, J=5.7 Hz) and 8.36 (t,J=6.0 Hz) (2t, 1H), 8.46 and 8.45 (2s, 1H), 8.23-8.17 (m, 1H), 7.67-7.03(m, 7H), 6.44-6.30 (m, 1H), 5.52 and 5.38 (2s, 2H), 4.62-4.22 (m, 3H),4.17 and 3.83 (2s, 2H), 2.59-2.53 (m, 1H), 1.21 (d, J=6.8 Hz) and 0.98(d, J=6.8 Hz) (2d, 6H), 0.68-0.59 (m, 2H), 0.47-0.37 (m, 2H); ¹⁹F NMR(282 MHz, DMSO) δ −121.22, −121.76; MS (ES+): 580.6 (M+Na); MS (ES−):558.5 (M−1).

Preparation of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-N-(pyridin-3-ylmethyl)-1H-indole-5-carboxamide(163a)

Reaction of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indole-5-carboxylicacid (129c) (50 mg, 0.1 mmol) with pyridin-3-ylmethanamine (0.015 mL,0.15 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column chromatography[silica (4 g), eluting with MeOH in DCM (1:0 to 19:1)]3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-N-(pyridin-3-ylmethyl)-1H-indole-5-carboxamide(163a) (42 mg, 71%) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) (amixture of two rotamers) δ 9.16-9.06 (m, 1H), 8.83 (t, J=5.7 Hz) and8.34 (t) (2t, 1H), 8.78-8.71 (m, 1H), 8.57 (bs, 1H), 8.49-8.43 (m, 1H),8.35 and 8.31 (2s, 1H), 7.83-6.91 (m, 7H), 5.40 and 5.21 (2s, 2H),4.63-4.54 and 4.29-4.21 (2m, 1H), 4.53 and 4.51 (2s, 2H), 4.47 (d, J=5.3Hz) and 4.33 (d, J=5.8 Hz) (2d, 2H), 4.19 and 3.85 (2s, 2H), 2.46 and2.45 (2s, 3H), 1.26 (d, J=6.4 Hz) and 1.00 (d, J=6.7 Hz) (2d, 6H); ¹⁹FNMR (282 MHz, DMSO-d₆) δ −121.19, −121.79; MS (ES+): 592.6 & 594.6(M+1).

Preparation of2-(3-acetyl-5-(pyrimidin-2-ylethynyl)-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(164a)

Reaction of2-(3-acetyl-5-bromo-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(158a) (300 mg, 0.56 mmol) using Cs₂CO₃ (365 mg, 1.12 mmol),dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine (X-PHOS, 53mg, 0.112 mmol), Pd₂(dba)₃ (51 mg, 0.056 mmol) according to procedurereported in Scheme 92 gave after workup and purification by flash columnchromatography [silica gel (8 g), eluting with MeOH in DCM from 0 to30%]2-(3-acetyl-5-(pyrimidin-2-ylethynyl)-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(164a) (21 mg, 0.038 mmol, 7% yield) as a dark-yellow solid; ¹H NMR (300MHz, DMSO-d₆) δ 8.87 (d, J=4.9 Hz, 2H), 8.49 (t, J=6.0 Hz, 1H),8.46-8.43 (m, 1H), 7.89-7.80 (m, 1H), 7.70 (dd, J=8.8, 1.5 Hz, 1H), 7.54(t, J=5.0 Hz, 1H), 7.46 (td, J=7.6, 1.7 Hz, 1H), 7.27-7.19 (m, 1H),7.14-7.07 (m, 1H), 5.81 (s, 2H), 4.34 (d, J=5.8 Hz, 2H), 4.00 (s, 2H),3.21-3.05 (m, 1H), 2.65 (s, 3H), 1.09-0.83 (m, 4H); ¹⁹F NMR (282 MHz,DMSO-d₆) δ −121.57; MS (ES+): 581.6, 583.6 (M+Na); MS (ES−): 593.5,595.6 (M+Cl).

Preparation of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-N-(pyridin-2-ylmethyl)-1H-indole-5-carboxamide(165c) Step-1: Preparation of methyl3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indole-5-carboxylate(165a)

Reaction of 2-(3-acetyl-5-(methoxycarbonyl)-1H-indol-1-yl)acetic acid(129a) (5.91 mmol, prepared according to the procedure reported byAltmann, Eva et al, in PCT Int. Appl., WO 2012/093101) withN-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide (10b) (1.82 g,7.09 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column [silica gel, elutingwith hexanes/10% MeOH in EtOAc (1:0 to 1:2)] methyl3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indole-5-carboxylate(165a) (1.89 g, 62%) as a light brown solid. ¹H NMR (300 MHz, DMSO-d₆) δ8.87 (dd, J=1.7, 0.6 Hz, 1H), 8.47 (t, J=5.9 Hz, 1H), 8.42 (s, 1H), 7.81(dd, J=8.7, 1.8 Hz, 1H), 7.58 (dd, J=8.7, 0.7 Hz, 1H), 7.49-7.41 (m,1H), 7.26-7.18 (m, 1H), 7.12-7.05 (m, 1H), 5.50 (s, 2H), 4.34 (d, J=5.8Hz, 2H), 3.99 (s, 2H), 3.88 (s, 3H), 3.16-3.04 (m, 1H), 2.46 (s, 3H),1.05-0.85 (m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.59; MS (ES+): 536.5& 538.5 (M+Na).

Step-2: Preparation of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indole-5-carboxylicacid (165b)

Reaction of methyl3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indole-5-carboxylate(165a) (1.83 g, 3.56 mmol) in THF (30 mL) and MeOH (30 mL) was added asolution of lithium hydroxide hydrate (911 mg, 21.28 mmol) in water (30mL) according to the procedure reported in step-2 of Scheme 129 gaveafter workup3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indole-5-carboxylicacid (165b) (1.51 g, 85%) as a light brown solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.83 (d, J=1.6 Hz, 1H), 8.48 (t, J=5.9 Hz, 1H), 8.38 (s, 1H),7.80 (dd, J=8.6, 1.7 Hz, 1H), 7.52 (d, J=8.7 Hz, 1H), 7.45 (td, J=7.6,1.7 Hz, 1H), 7.27-7.18 (m, 1H), 7.12-7.05 (m, 1H), 5.48 (s, 2H), 4.34(d, J=5.7 Hz, 2H), 3.99 (s, 2H), 3.15-3.03 (m, 1H), 2.45 (s, 3H),1.06-0.82 (m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.59; MS (ES+): 522.5(M+Na); MS (ES−): 534.5 & 536.5 (M+Cl).

Step-3: Preparation of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-N-(pyridin-2-ylmethyl)-1H-indole-5-carboxamide(165c)

Reaction of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indole-5-carboxylicacid (165b) (50 mg, 0.1 mmol) with pyridin-2-ylmethanamine (0.015 mL,0.15 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column chromatography[silica (4 g), eluting with MeOH in DCM (1:0 to 19:1)]3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-N-(pyridin-2-ylmethyl)-1H-indole-5-carboxamide(165c) (45 mg, 76%) as a light yellow solid; ¹H NMR (300 MHz, DMSO-d₆)(a mixture of two rotamers) δ 9.13 (t, J=5.9 Hz, 1H), 8.80-8.78 (m, 1H),8.53-8.50 (m, 1H), 8.47 (t, J=5.9 Hz, 1H), 8.38 (s, 1H), 7.83-7.70 (m,2H), 7.54 (d, J=8.7 Hz, 1H), 7.48-7.41 (m, 1H), 7.32 (d, J=7.9 Hz, 1H),7.29-7.19 (m, 2H), 7.09 (t, J=7.9 Hz, 1H), 5.49 (s, 2H), 4.59 (d, J=5.8Hz, 2H), 4.35 (d, J=5.7 Hz, 2H), 4.00 (s, 2H), 3.15-3.06 (m, 1H), 2.46(s, 3H), 1.05-0.88 (m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.60; MS(ES+): 590.6 (M+1) & 612.6 (M+Na).

Preparation of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-N-(pyridin-4-ylmethyl)-1H-indole-5-carboxamide(166a)

Reaction of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indole-5-carboxylicacid (165b) (50 mg, 0.1 mmol) with pyridin-4-ylmethanamine (0.016 mL,0.15 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column chromatography[silica (4 g), eluting with MeOH in DCM (1:0 to 19:1)]3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-N-(pyridin-4-ylmethyl)-1H-indole-5-carboxamide(166a) (27 mg, 46%) as an off-white solid; ¹H NMR (300 MHz, DMSO-d₆) (amixture of two rotamers) δ 9.15 (t, J=5.9 Hz, 1H), 8.79-8.77 (m, 1H),8.54-8.43 (m, 3H), 8.38 (s, 1H), 7.78 (dd, J=8.7, 1.8 Hz, 1H), 7.55 (d,J=8.6 Hz, 1H), 7.49-7.41 (m, 1H), 7.34-7.29 (m, 2H), 7.27-7.18 (m, 1H),7.14-7.02 (m, 1H), 5.49 (s, 2H), 4.52 (d, J=5.9 Hz, 2H), 4.35 (d, J=5.8Hz, 2H), 4.00 (s, 2H), 3.17-3.03 (m, 1H), 2.46 (s, 3H), 1.08-0.74 (m,4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.59; MS (ES+): 590.7 & 592.7(M+1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-(methylsulfonyl)azetidin-3-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(167b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-((1-(methylsulfonyl)azetidin-3-yl)amino)acetamide(167a)

Reaction of 2-bromo-N-(3-chloro-2-fluorobenzyl)acetamide (69b) (250 mg,0.89 mmol) with 1-(methylsulfonyl)azetidin-3-amine (241 mg, 1.60 mmol)according to the procedure reported in step-2 of Scheme 35 gave afterworkup and purification by flash column chromatography [Silica gel, (12g) eluting with MeOH in DCM, 0-30%) to affordN-(3-chloro-2-fluorobenzyl)-2-((1-(methylsulfonyl)azetidin-3-yl)-amino)acetamide(167a) (68 mg, 0.194 mmol, 22% yield) as a thick yellow oil which wasused as such in the next step; MS (ES+): 350.4 (M+1), 372.4 (M+Na); MS(ES−): 348.3 (M−1), 384.3, 386.3 (M+Cl)

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-(methylsulfonyl)azetidin-3-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(167b)

Reaction ofN-(3-chloro-2-fluorobenzyl)-2-((1-(methylsulfonyl)azetidin-3-yl)amino)acetamide(167a) (30 mg, 0.086 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (19 mg, 0.086 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [Silica gel, (8 g) eluting with MeOH in DCM from 0-30%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-(methylsulfonyl)azetidin-3-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(167b) (8 mg, 0.015 mmol, 17% yield) as a white solid as a mixture oftwo rotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 8.99 (t, J=5.7 Hz) & 8.64 (t,J=5.8 Hz) (2t, 1H), 8.22-8.12 (m, 1H), 7.74-7.66 (m, 2H), 7.62-6.95 (m,6H), 5.64 & 5.42 (s, 2H), 5.19-4.76 (m, 1H), 4.49 (d, J=5.6 Hz) & 4.34(d, J=5.8 Hz) (2d, 2H), 4.42 (s) and 4.23-3.78 (m) (6H), 3.08 & 2.99 (s,3H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.32, −121.65; MS (ES+): 551.52(M+1), 573.5 (M+Na); MS (ES−): 549.5 (M−1), 585.3 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((3-ethyloxetan-3-yl)methyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(168b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-((2-(3-ethyloxetan-3-yl)methyl)amino)acetamide(168a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (205 mg,0.87 mmol) with (3-ethyloxetan-3-yl)methanamine (250 mg, 2.47 mmol)according to the procedure reported in step-2 of Scheme 35 gave afterworkupN-(3-chloro-2-fluorobenzyl)-2-((2-(3-ethyloxetan-3-yl)methyl)amino)acetamide(168a) as a colorless oil which was used in the next step withoutfurther purification; MS (ES+) 315.4 (M+1); (ES−) 313.4 (M−1).

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((3-ethyloxetan-3-yl)methyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(168b)

Reaction ofN-(3-chloro-2-fluorobenzyl)-2-((2-(3-ethyloxetan-3-yl)methyl)amino)acetamide(168a) (51 mg, 0.162 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (43 mg, 0.19 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with DMA-80 in DCM 0 to 100%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((3-ethyloxetan-3-yl)methyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(168b) (26 mg, 0.05 mmol, 31% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.84 (t, J=5.7 Hz) and 8.51 (t) (1H), 8.18 (dt, J=8.1, 1.0Hz, 1H), 7.79-7.00 (m, 8H), 5.51 and 5.50 (2s, 2H), 4.47 (d, J=5.5 Hz)and 4.40-3.73 (m) (8H), 1.74 (q) and 1.61 (q, J=7.3 Hz, 2H), 1.09 (t,J=7.3 Hz) and 0.84 (t, J=7.4 Hz) (3H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.17, −121.55; MS (ES+): 516.5 (M+1); MS (ES−): 514.5 (M−1).

Preparation of1-(2-(((trans)-3-aminocyclobutyl)(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(169c) Step-1: Preparation of tert-butyl((trans)-3-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)cyclobutyl)carbamate(169a)

Reaction of 2-bromo-N-(3-chloro-2-fluorobenzyl)acetamide (69b) (250 mg,0.89 mmol) with tert-butyl (trans)-3-aminocyclobutylcarbamate (250 mg,1.34 mmol) according to the procedure reported in step-2 of Scheme 35gave tert-butyl((trans)-3-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)cyclobutyl)carbamate(169a) (173 mg, 0.45 mmol, 50% yield) as a thick yellow oil; MS (ES+):386.5 (M+1), 408.5 (M+Na); MS (ES−): 384.4 (M−1), 420.4, 422.4 (M+Cl).

Step-2: Preparation of tert-butyl((trans)-3-(2-(3-carbamoyl-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)acetamido)cyclobutyl)carbamate(169b)

Reaction of tert-butyl((trans)-3-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)cyclobutyl)carbamate(169a) (108 mg, 0.28 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (74 mg, 0.34 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [Silica gel, (24 g) eluting with MeOH in CHCl₃ 0-10%]tert-butyl((trans)-3-(2-(3-carbamoyl-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)acetamido)cyclobutyl)carbamate(169b) (0.101 g, 0.172 mmol, 61.5% yield) as an off-white solid in theform of mixture two rotamers; MS (ES+): 587.6 (M+1), 609.6, 611.6(M+Na); MS (ES−): 585.6 (M−1), 621.6, 623.6 (M+Cl).

Step-3: Preparation of1-(2-(((trans)-3-aminocyclobutyl)(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(169c)

Reaction oftert-butyl((trans)-3-(2-(3-carbamoyl-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)acetamido)cyclobutyl)carbamate(169b) (91 mg, 0.16 mmol) with TFA (0.24 mL, 3.1 mmol) according to theprocedure reported in step-2 of Scheme 2 gave after workup andpurification by flash column chromatography [Silica gel, (12 g) elutingwith DMA80 in DCM 0-100%)]1-(2-(((trans)-3-aminocyclobutyl)(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(169c) (17 mg, 22% yield) as a white solid as a mixture of two isomers;¹H NMR (300 MHz, DMSO-d₆) δ 8.88 (t, J=5.8 Hz) & 8.43 (t, J=5.9 Hz) (2t,1H, D₂O exchangeable), 8.21-8.14 (m, 1H), 7.72 (s, 1H), 7.63-7.02 (m,7H), 5.53 & 5.42 (2s, 2H), 5.06-4.81 (m, 1H), 4.47 (d, J=5.6 Hz) & 4.33(d, J=5.8 Hz) (2d, 2H), 4.29 & 4.01 (2s, 2H), 2.42-1.69 (m, 4H); ¹⁹F NMR(282 MHz, DMSO-d₆) δ −121.25, −121.64; MS (ES+): 487.5 (M+1), 509.5(M+Na); MS (ES−): 485.5 (M−1), 521.43 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((trans)-3-methoxycyclobutyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(170b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-(((trans)-3-methoxycyclobutyl)amino)acetamide(170a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (195 mg,0.826 mmol) with trans-3-methoxycyclobutanamine hydrochloride (250 mg,1.82 mmol) according to the procedure reported in step-2 of Scheme 35gave after workup and purification by flash column chromatography[silica (12 g), eluting with EtOAc/MeOH (9:1) in hexane 0 to 60%]N-(3-chloro-2-fluorobenzyl)-2-(((trans)-3-methoxycyclobutyl)amino)acetamide(170a) (122 mg, 0.41 mmol, 50%) as a colorless oil; MS (ES+) 301.4(M+1); MS (ES−): 299.3 (M−1).

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((trans)-3-methoxycyclobutyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(170b)

Reaction ofN-(3-chloro-2-fluorobenzyl)-2-(((trans)-3-methoxycyclobutyl)amino)acetamide(170a) (122 mg, 0.41 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (122 mg, 0.41 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with CMA-80 in CHCl₃ 0 to 60%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((trans)-3-methoxycyclobutyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(170b) (137 mg, 0.27 mmol, 67% yield) as an off white solid; ¹H NMR (300MHz, DMSO-d₆) δ 8.87 (t, J=5.7 Hz) and 8.44 (t, J=5.9 Hz) (2t, 1H), 8.17(d, J=8.1 Hz, 1H), 7.72-7.01 (m, 8H), 5.55 and 5.42 (2s, 2H), 4.85-4.69(m, 1H), 4.47 (d, J=5.6 Hz) and 4.33 (d, J=5.7 Hz) (2d, 2H), 4.29 and,4.02 (2s, 2H), 3.92-3.78 (m, 1H), 3.17 and 3.10 (2s, 3H), 2.43-1.93 (m,4H); ¹⁹F NMR (282 MHz, DMSO) δ −121.18, −121.60; MS (ES+) 502.5 (M+1);524.5 (M+Na); (ES−) 500.5 (M−1); (Based on NMR, this compound is amixture of rotamers 4:5 ratio).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((trans)-3-hydroxy-3-(cis)-methylcyclobutyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(171b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-(((trans)-3-hydroxy-3-(cis)-methylcyclobutyl)amino)acetamide(171a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (195 mg,0.83 mmol) with (trans)-3-amino-1-methylcyclobutanol hydrochloride (250mg, 1.82 mmol) according to the procedure reported in step-2 of Scheme35 gave after workup and purification by flash column chromatography[silica (12 g), eluting with EtOAc/MeOH (9:1) in hexane 0 to 60%] ofN-(3-chloro-2-fluorobenzyl)-2-(((trans)-3-hydroxy-3-(cis)-methylcyclobutyl)amino)acetamide(171a) (108 mg, 0.36 mmol, 43%) as a colorless oil; ¹H NMR (300 MHz,DMSO-d₆) δ 8.33 (t, J=6.1 Hz, 1H), 7.48 (td, J=7.6, 1.9 Hz, 1H),7.31-7.24 (m, 1H), 7.23-7.15 (m, 1H), 4.69 (s, 1H), 4.36 (d, J=5.9 Hz,2H), 3.17 (d, J=4.7 Hz, 2H), 3.03 (s, 2H), 2.14-2.03 (m, 2H), 1.70-1.58(m, 2H), 1.23 (s, 3H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.65; MS (ES+)3001.4 (M+1), 323.4 (M+Na); (ES−) 299.3 (M−1).

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((trans)-3-hydroxy-3-(cis)-methylcyclobutyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(171b)

Reaction ofN-(3-chloro-2-fluorobenzyl)-2-(((trans)-3-hydroxy-3-(cis)-methylcyclobutyl)amino)acetamide(171a) (108 mg, 0.36 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (87 mg, 0.4 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with CMA-80 in CHCl₃ 0 to 60%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((trans)-3-hydroxy-3-(cis)-methylcyclobutyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(171b) (65 mg, 0.13 mmol, 36% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.88 (t, J=5.7 Hz) and 8.42 (t, J=5.9 Hz) (2t, 1H), 8.17 (m,1H), 7.69 (m, 1H), 7.31-7.01 (m, 7H), 5.53 and 5.42 (2s, 2H), 5.01-4.67(m, 2H), 4.46 (d, J=5.5 Hz) and 4.33 (d, J=5.8 Hz) (2d, 2H), 4.24 and3.99 (2s, 2H), 2.32-1.83 (m, 4H), 1.26 and 1.17 (2s, 3H); ¹⁹F NMR (282MHz, DMSO) δ −121.09, −121.56; MS (ES+) 524.5 (M+Na); (ES−): 500.5(M−1); (Based on NMR, this compound is a mixture of rotamers 1:1 ratio).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(((trans)-3-hydroxycyclobutyl)methyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(172b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-((((trans)-3-hydroxycyclobutyl)methyl)amino)acetamide(172a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (254 mg,1.08 mmol) with (trans)-3-(aminomethyl)cyclobutanol hydrochloride (370mg, 2.69 mmol) according to the procedure reported in step-2 of Scheme35 gave after workup and purification by flash column chromatography[silica (12 g), eluting with EtOAc/MeOH (9:1) in hexane 0 to 60%] ofN-(3-chloro-2-fluorobenzyl)-2-((((trans)-3-hydroxycyclobutyl)methyl)amino)acetamide(172a) (130 mg, 0.43 mmol, 40%) as a colorless oil; MS (ES+): 301.4,303.4 (M+1, M+2), 323.3 (M+Na); MS (ES⁻) 299.3 (M−1).

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(((trans)-3-hydroxycyclobutyl)methyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(172b)

Reaction ofN-(3-chloro-2-fluorobenzyl)-2-((((trans)-3-hydroxycyclobutyl)methyl)amino)acetamide(172a) (130 mg, 0.43 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (104 mg, 0.48 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with CMA-80 in CHCl₃ 0 to 60%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(((trans)-3-hydroxycyclobutyl)methyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(172b) (32 mg, 0.064 mmol, 15% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.81 (t, J=5.8 Hz) and 8.45 (t, J=6.0 Hz) (2t, 1H), 8.21-8.13(m, 1H), 7.73 (bs, 1H), 7.58-7.07 (m, 7H), 5.57 and 5.47 (2s, 2H), 5.05(d, J=6.1 Hz) and 4.93 (d, J=6.0 Hz) (2d, 1H), 4.45 (d, J=5.5 Hz) and4.32 (d, J=6.0 Hz) (2d, 2H), 4.23 and 3.93 (2s, 2H), 4.41-4.25 and4.19-4.07 (2m, 1H), 3.56 (d, J=8.0 Hz) and 3.31 (d, J=7.9 Hz) (2d, 2H),2.32-1.76 (m, 5H); ¹⁹F NMR (282 MHz, DMSO) δ −121.27, −121.65; MS (ES+)524.5 (M+Na); (ES−) 500.5 (M−1). (Based on NMR, this compound is amixture of rotamers 2:1 ratio)

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((tran)-4-hydroxycyclohexyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(173b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-(((trans)-4-hydroxycyclohexyl)amino)acetamide(173a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (342 mg,1.45 mmol) with (trans)-4-aminocyclohexanol (500 mg, 4.34 mmol)according to the procedure reported in step-2 of Scheme 35 gave afterworkup and purification by flash column chromatography [silica (12 g),eluting with EtOAc/MeOH (9:1) in hexane 0 to 60%] ofN-(3-chloro-2-fluorobenzyl)-2-(((trans)-4-hydroxycyclohexyl)amino)acetamide(173a) (445 mg, 1.41 mmol, 98%) as a colorless oil; MS (ES+): 315.4,317.4 (M+1, M+3); (ES−): 313.3.

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((tran)-4-hydroxycyclohexyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(173b)

Reaction ofN-(3-chloro-2-fluorobenzyl)-2-(((trans)-4-hydroxycyclohexyl)amino)acetamide(173a) (320 mg, 1.02 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (245 mg, 1.12 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with CMA80 in CHCl₃ 0 to 60%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((tran)-4-hydroxycyclohexyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(173b) (110 mg, 0.21 mmol, 21% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.80 (t, J=5.7 Hz) and 8.33 (t, J=6.0 Hz) (2t, 1H), 8.21-8.14(m, 1H), 7.75-7.64 (m, 1H), 7.63-7.00 (m, 7H), 5.61 and 5.45 (2s, 2H),4.60 (d, J=4.2 Hz) and 4.55 (d, J=4.6 Hz) (2d, 1H), 4.45 (d, J=5.6 Hz)and 4.31 (d, J=5.8 Hz) (2d, 2H), 4.24-3.72 (m, 3H), 3.45-3.19 (m, 1H),1.94-0.98 (m, 8H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.13, −121.69; MS(ES+): 516.5 (M+1), 538.5 (M+Na); (ES−): 514.5 (M−1), 550.5 (M+Cl);(Based on NMR, this compound is a mixture of rotamers 3:2 ratio).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-N5-(cyclopropylmethyl)-1H-indazole-3,5-dicarboxamide)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-N-(pyri din-3-ylmethyl)-1H-indole-5-carboxamide (174a)

Reaction of3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (144a) (50 mg, 0.1 mmol) with cyclopropylmethanamine (0.013 mL,0.15 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column chromatography[silica (4 g), eluting with MeOH in DCM (1:0 to 19:1)]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-N5-(cyclopropylmethyl)-1H-indazole-3,5-dicarboxamide)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-N-(pyridin-3-ylmethyl)-1H-indole-5-carboxamide(174a) (31 mg, 56%) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) (amixture of two rotamers) δ 8.83 (t, J=5.7 Hz) and 8.37 (t, J=5.9 Hz)(2t, 1H), 8.77-8.62 (m, 2H), 7.93-6.94 (m, 7H), 5.62 and 5.48 (2s, 2H),4.61-4.48 and 4.29-4.20 2 (m, 1H), 4.46 (d, J=5.6 Hz) and 4.31 (d, J=5.8Hz) (2d, 2H), 4.18 and 3.83 (2s, 2H), 3.17 (t, J=6.3 Hz, 2H), 1.23 (d,J=6.3 Hz) and 0.99 (d, J=6.8 Hz) (2d, 6H), 1.13-1.01 (m, 1H), 0.51-0.37(m, 2H), 0.32-0.18 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.22,−121.73; MS (ES+): 557.6 (M+1) & 579.6 (M+Na); MS (ES−): 591.5 & 593.5(M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-N5-(1-phenylethyl)-1H-indazole-3,5-dicarboxamide(175a)

Reaction of3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (144a) (50 mg, 0.1 mmol) with 1-phenylethanamine (0.02 mL, 0.15mmol) according to the procedure reported in step-3 of Scheme 2 gaveafter workup and purification by flash column chromatography [silica (4g), eluting with MeOH in DCM (1:0 to 19:1)]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-N5-(1-phenylethyl)-1H-indazole-3,5-dicarboxamide(175a) (49 mg, 81%) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) (amixture of two rotamers) δ 9.02 (d, J=3.6 Hz) and 8.99 (d, J=3.8 Hz)(2d, 1H), 8.83 (t, J=5.7 Hz) and 8.36 (t, J=5.9 Hz) (2t, 1H), 8.77-8.71(m, 1H), 7.97-6.94 (m, 12H), 5.62 and 5.48 (2s, 2H), 5.29-5.09 (m, 1H),4.62-4.49 and 4.28-4.21 (2m, 1H), 4.46 (d, J=5.6 Hz) and 4.31 (d, J=5.9Hz) (2d, 2H), 4.18 and 3.83 (2s, 2H), 1.55-1.46 (m, 3H), 1.23 (d, J=6.3Hz) and 0.99 (d, J=6.9 Hz) (2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.22, −121.73; MS (ES+): 607.7 (M+1) & 629.7 (M+Na); MS (ES−): 641.6& 643.6 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-N5-(pyrimidin-5-yl)-1H-indazole-3,5-dicarboxamide(176a)

Reaction of3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (144a) (50 mg, 0.1 mmol) with pyrimidin-5-amine (15 mg, 0.15 mmol)according to the procedure reported in step-3 of Scheme 2 gave afterworkup and purification by flash column chromatography [silica (4 g),eluting with MeOH in DCM (1:0 to 9:1)]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-N5-(pyrimidin-5-yl)-1H-indazole-3,5-dicarboxamide(176a) (10 mg, 17%) as an off-white solid; ¹H NMR (300 MHz, DMSO-d₆) (amixture of two rotamers) δ 10.863 and 10.857 (2s, 1H), 9.213 and 9.209(2s, 2H), 8.941 and 8.938 (2s, 1H), 8.93-8.82 (m, 2H), 8.49-6.91 (m,7H), 5.67 and 5.53 (2s, 2H), 4.66-4.50 and 4.29-4.22 (2m, 1H), 4.47 (d,J=5.5 Hz) and 4.32 (d, J=6.0 Hz) (2d, 2H), 4.20 and 3.85 (2s, 2H), 1.24(d, J=6.6 Hz) and 1.00 (d, J=6.8 Hz) (2d, 6H); ¹⁹F NMR (282 MHz,DMSO-d₆) δ −121.21, −121.70; MS (ES+): 581.6 (M+1); 603.6 (M+Na).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(piperidine-1-carboxamido)-1H-indazole-3-carboxamide(177a)

Reaction of3-carbamoyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (145a) (420 mg, 0.79 mmol) in toluene (15 mL) with piperidine (135mg, 1.59 mmol) using TEA (0.44 mL, 3.18 mmol) as base according to theprocedure reported in step-4 of Scheme 129 gave after workup andpurification by column chromatography [silica gel (12 g), eluting withDMA80 in DCM 0 to 40%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(piperidine-1-carboxamido)-1H-indazole-3-carboxamide(177a) (179 mg, 0.31 mmol, 39% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.82 (t, J=5.7 Hz) and 8.37 (t, J=5.9 Hz) (2t, 1H), 8.58 (s,1H), 8.22-8.15 (m, 1H), 7.66-7.06 (m, 7H), 5.53 and 5.40 (2s, 2H),4.63-4.23 (m, 3H), 4.17 and, 3.83 (2s, 2H), 3.48-3.39 (m, 4H), 1.65-1.42(m, 6H), 1.21 (d, J=6.5 Hz) and 0.99 (d, J=6.8 Hz) (2d, 6H); ¹⁹F NMR(282 MHz, DMSO-d₆) δ −121.22, −121.78; MS (ES+) 586.6 (M+1); MS (ES−)584.5 (M−1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(4,4-difluoropiperidine-1-carboxamido)-1H-indazole-3-carboxamide(178a)

Reaction of3-carbamoyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (145a) (150 mg, 0.28 mmol) in toluene (10 mL) with4,4-difluoropiperidine hydrochloride (134 mg, 0.85 mmol) using TEA (0.16mL, 1.13 mmol) as base according to the procedure reported in step-4 ofScheme 129 gave after workup and purification by column chromatography[silica gel (12 g), eluting with DMA80 in DCM 0 to 40%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(4,4-difluoropiperidine-1-carboxamido)-1H-indazole-3-carboxamide(178a) (43 mg, 0.069 mmol, 24% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.91-8.32 (m, 2H), 8.23-8.14 (m, 1H), 7.66-7.06 (m, 7H), 5.53and 5.40 (2s, 2H), 4.62-4.23 (m, 3H), 4.17 and 3.83 (2s, 2H), 3.66-3.56(m, 4H), 2.09-1.87 (m, 4H), 1.21 (d, J=6.5 Hz) and 0.99 (d, J=6.8 Hz)(2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −95.19, −121.22, −121.78; MS(ES+): 622.6 (M+1); MS (ES−): 620.5 (M−1).

Preparation of2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(179c) Step-1: Preparation of tert-butyl2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indazol-1-yl)acetate (179a)

Reaction of tert-butyl 2-(3-acetyl-5-bromo-1H-indazol-1-yl)acetate(156d) (1.0 g, 2.83 mmol) with pyrimidin-5-amine (0.539 g, 5.66 mmol)according to the procedure reported in step-1 of Scheme 97 gave afterworkup and purification by flash column chromatography [silica gel (40g), eluting with DMA80 in DCM 0 to 20%] tert-butyl2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indazol-1-yl)acetate (179a) (720mg, 1.96 mmol, 69% yield) as an off-white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.73 (s, 1H), 8.65 (s, 1H), 8.56 (s, 2H), 7.93-7.88 (m, 1H),7.72 (dd, J=9.0, 0.7 Hz, 1H), 7.37 (dd, J=9.1, 2.2 Hz, 1H), 5.42 (s,2H), 2.59 (s, 3H), 1.44 (s, 9H); MS (ES+): 368.5 (M+1), 390.5 (M+Na); MS(ES−): 366.5 (M−1), 402.4 (M+Cl).

Step-2: Preparation of2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indazol-1-yl)acetic acid (179b)

Reaction of tert-butyl2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indazol-1-yl)acetate (179a) (700mg, 1.91 mmol) with TFA (1.47 mL, 19.05 mmol) according to the procedurereported in step-2 of Scheme 2 gave after workup and trituration with30% EtOAc-hexane (10 mL)2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indazol-1-yl)acetic acid (179b)(400 mg, 1.35 mmol, 99% yield) as an off-white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 13.37 (s, 1H, D₂O exchangeable), 8.74 (s, 1H), 8.66 (s, 1H),8.56 (s, 2H), 7.90 (dd, J=2.2, 0.7 Hz, 1H), 7.76 (dd, J=9.0, 0.7 Hz,1H), 7.36 (dd, J=9.0, 2.2 Hz, 1H), 5.43 (s, 2H), 2.59 (s, 3H); MS (ES+):312.4 (M+1), 334.4 (M+Na), MS (ES−): 310.4 (M−1).

Step-3: Preparation of2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(179c)

Reaction of 2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indazol-1-yl)aceticacid (179b) (70 mg, 0.23 mmol) withN-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide (19c) (58 mg,0.23 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column [silica gel (12 g),eluting with DMA-80 in DCM 0-20%]2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(179c) (105 mg, 0.19 mmol, 85% yield) as a very light orange solid as amixture of two rotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 8.84 and 8.36 (2t,J=5.6 Hz, 1H), 8.72 (s, 1H), 8.65 and 8.64 (2s, 1H), 8.55 (s, 2H), 7.908and 7.902 (2s, 1H), 7.70-7.00 (m, 5H), 5.67 and 5.51 (2s, 2H), 4.63-4.52and 4.33-4.20 (2m, 1H), 4.47 and 4.33 (2d, J=6.0 Hz, 2H), 4.18 and 3.85(2s, 2H), 2.59 (s, 3H), 1.25 and 1.00 (2d, J=6.8 Hz, 6H); ¹⁹F NMR (282MHz, DMSO-d₆) δ −121.21, −121.72; MS (ES+): 552.6 (M+1); MS (ES−):586.5, 588.5 (M+Cl).

Preparation of2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indazol-1-yl)-N-(2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)-N-isopropylacetamide(180a)

Reaction of 2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indazol-1-yl)aceticacid (179b) (70 mg, 0.23 mmol) withN-(2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-2-(isopropylamino)acetamide(115c) (72 mg, 0.23 mmol) according to the procedure reported in step-3of scheme-2 gave after workup and purification by flash column [silicagel (12 g), eluting with DMA-80 in DCM 0-20%]2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indazol-1-yl)-N-(2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)-N-isopropylacetamide(180a) (61 mg, 0.099 mmol, 44% yield) as an off-white solid as a mixtureof two rotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 10.27 and 9.76 (2s, 1H),8.73 and 8.72 (2s, 1H), 8.65 (s, 1H), 8.55 and 8.54 (2s, 2H), 8.11 and7.95 (2t, J=7.4 Hz, 1H), 7.90 and 7.89 (2d, J=2.1 Hz, 1H), 7.68-7.00 (m,6H), 5.73 and 5.55 (2s, 2H), 4.73-4.57 and 4.40-4.26 (2m, 1H), 4.47 and4.09 (2s, 2H), 2.59 and 2.58 (2s, 3H), 1.28 and 1.07 (2d, J=6.8 Hz, 6H);¹⁹F NMR (282 MHz, DMSO-d₆) δ −126.81, −126.96; MS (ES+): 614.6 (M+1); MS(ES−): 648.6 (M+Cl).

Preparation of(S)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(pentan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(181b) Step-1: Preparation of(S)—N-(3-chloro-2-fluorobenzyl)-2-(pentan-2-ylamino)acetamide (181a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (267 mg,1.13 mmol) with (S)-pentan-2-amine hydrochloride (350 mg, 2.83 mmol)according to the procedure reported in step-2 of Scheme 35 gave afterworkup and purification by flash column chromatography [silica (12 g),eluting with EtOAc/MeOH (9:1) in hexane 0 to 60%](S)—N-(3-chloro-2-fluorobenzyl)-2-(pentan-2-ylamino)acetamide (181a)(112 mg, 0.39 mmol, 35%) as a colorless oil; MS (ES+): 287.4, 289.4(M+1, M+3); (ES−): 285.4.

Step-2: Preparation of(S)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(pentan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(181b)

Reaction of(S)—N-(3-chloro-2-fluorobenzyl)-2-(pentan-2-ylamino)acetamide (181a)(112 mg, 0.39 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e)(94 mg, 0.43 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with DMA80 in DCM 0 to 60%](S)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(pentan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(181b) (141 mg, 0.29 mmol, 74% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) (a mixture of two rotamers) δ 8.81 (t, J=5.6 Hz) and 8.34 (t,J=6.2 Hz) (2t, 1H), 8.22-8.13 (m, 1H), 7.70 (bs, 1H), 7.59-7.04 (m, 7H),5.63-5.40 (m, 2H), 4.56-3.70 (m, 5H), 1.62-0.58 (m, 10H); ¹⁹F NMR (282MHz, DMSO-d₆) δ −121.19, −121.73; MS (ES+): 488.5 (M+1); MS (ES−): 486.5(M−1).

Preparation of2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-(trans-3-hydroxycyclobutyl)acetamide(182a)

Reaction of 2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indazol-1-yl)aceticacid (179b) (70 mg, 0.23 mmol) withN-(3-chloro-2-fluorobenzyl)-2-(((trans)-3-hydroxycyclobutyl)amino)acetamide(110a) (64 mg, 0.23 mmol) according to the procedure reported in step-3of scheme-2 gave after workup and purification by flash column [silicagel (12 g), eluting with DMA-80 in DCM 0-50%]2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-(trans-3-hydroxycyclobutyl)acetamide(182a) (65 mg, 0.11 mmol, 50% yield) as a off-white solid; ¹H NMR (300MHz, DMSO-d₆) (a mixture of two rotamers) δ 8.87 and 8.43 (2t, J=5.7 Hz,1H), 8.728 and 8.72 (2s, 1H), 8.657 and 8.65 (2s, 1H), 8.55 (s, 2H),7.90 and 7.89 (2s, 1H), 7.67-7.03 (m, 5H), 5.61 and 5.48 (2s, 2H), 5.10and 5.02 (2d, J=4.0 Hz, 1H), 4.96 and 4.86 (2t, J=8.2 Hz, 1H), 4.47 and4.34 (2d, J=5.6 Hz, 2H), 4.27 and 4.02 (2s, 2H), 4.24-4.09 (m, 1H),2.587 and 2.58 (2s, 3H), 2.46-2.33 (m, 1H), 2.29-2.12 (m, 2H), 2.02-1.88(m, 1H); 19F NMR (282 MHz, DMSO-d₆) (a mixture of two rotamers) δ−121.22, −121.59; MS (ES+):

580.6 (M+1), 602.5 (M+Na); MS (ES−): 614.5 (M+Cl).

Preparation of2-(3-acetyl-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-(trans-3-hydroxycyclobutyl)acetamide(183a)

Reaction of 2-(3-acetyl-1H-indazol-1-yl)acetic acid (155c) (70 mg, 0.32mmol) withN-(3-chloro-2-fluorobenzyl)-2-(((trans)-3-hydroxycyclobutyl)amino)acetamide(110a) (92 mg, 0.32 mmol) according to the procedure reported in step-3of scheme-2 gave after workup and purification by flash column [silicagel (12 g), eluting with DMA-80 in DCM 0-40%]2-(3-acetyl-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-(trans-3-hydroxycyclobutyl)acetamide(183a) (70 mg, 0.14 mmol, 45% yield) as a off-white solid; ¹H NMR (300MHz, DMSO-d₆) (mixture of two rotamers) δ 8.87 and 8.42 (2t, J=5.9 Hz,1H), 8.20 and 8.17 (2d, J=1.0 Hz, 1H), 7.72-6.99 (m, 6H), 5.63 and 5.50(2s, 2H), 5.10 and 5.01 (2d, J=4.4 Hz, 1H), 4.98-4.80 (m, 1H), 4.47 and4.33 (2d, J=5.8 Hz, 2H), 4.28 and 4.01 (2s, 2H) 4.24-4.09 (m, 1H), 2.61(s, 3H), 2.46-2.34 (m, 1H), 2.29-2.13 (m, 2H), 2.00-1.88 (m, 1H); ¹⁹FNMR (282 MHz, DMSO-d₆) (mixture of two rotamers) δ −121.23, −121.63; MS(ES+): 487.5 (M+1): MS (ES−): 521.4 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(3-methylbutan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(184b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-((3-methylbutan-2-yl)amino)acetamide(184a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (316 mg,1.34 mmol) with 3-methylbutan-2-amine (350 mg, 4.02 mmol) according tothe procedure reported in step-2 of Scheme 35 gave after workup andpurification by flash column chromatography [silica (12 g), eluting withEtOAc/MeOH (9:1) in hexane 0 to 60%]N-(3-chloro-2-fluorobenzyl)-2-((3-methylbutan-2-yl)amino)acetamide(184a) (145 mg, 0.51 mmol, 38%) as a colorless oil; ¹H NMR (300 MHz,DMSO-d₆) δ 8.32 (t, J=6.1 Hz, 1H), 7.46 (ddd, J=7.9, 7.2, 1.8 Hz, 1H),7.32-7.23 (m, 1H), 7.22-7.12 (m, 1H), 4.48-4.29 (m, 2H), 3.22-3.05 (m,2H), 2.40-2.24 (m, 1H), 1.99 (s, 1H), 1.68-1.53 (m, 1H), 0.86-0.77 (m,9H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.62; MS (ES+): 287.4 (M+1); MS(ES−): 285.3 (M−1).

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(3-methylbutan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(184b)

Reaction ofN-(3-chloro-2-fluorobenzyl)-2-((3-methylbutan-2-yl)amino)acetamide(184a) (145 mg, 0.51 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (122 mg, 0.56 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with DMA80 in DCM 0 to 60%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(3-methylbutan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(184b) (113 mg, 0.23 mmol, 46% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) (mixture of two rotamers) δ 8.81 (t, J=5.7 Hz) and 8.34 (t,J=6.0 Hz) (2t, 1H), 8.23-8.13 (m, 1H), 7.77-7.66 (m, 1H), 7.58-7.15 (m,7H), 5.72-5.36 (m, 2H), 4.54-3.63 (m, 5H), 1.82-1.55 (m, 1H), 1.26 (d,J=6.4 Hz) and 1.01-0.93 (m) and 0.84 (d, J=6.5 Hz) and 0.74 (d, J=6.5 Hz(9H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.20, −121.80; MS (ES+) 488.5(M+1); MS (ES−) 486.5 (M−1).

Preparation of(S)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(tetrahydrofuran-3-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(185b) Step-1: Preparation of(S)—N-(3-chloro-2-fluorobenzyl)-2-((tetrahydrofuran-3-yl)amino)acetamide(185a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (325 mg,1.38 mmol) with (S)-tetrahydrofuran-3-amine (300 mg, 3.44 mmol)according to the procedure reported in step-2 of Scheme 35 gave afterworkup and purification by flash column chromatography [silica (12 g),eluting with EtOAc/MeOH (9:1) in hexane 0 to 60%](S)—N-(3-chloro-2-fluorobenzyl)-2-((tetrahydrofuran-3-yl)-amino)acetamide(185a) (112 mg, 0.39 mmol, 28%) as a colorless oil; MS (ES+): 287.4(M+1), 309.3 (M+Na); MS (ES−): 285.3

Step-2: Preparation of(S)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(tetrahydrofuran-3-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(185b)

Reaction of(S)—N-(3-chloro-2-fluorobenzyl)-2-((tetrahydrofuran-3-yl)amino)acetamide(185a) (112 mg, 0.39 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (94 mg, 0.43 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with DMA80 in DCM 0 to 60%](S)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(tetrahydrofuran-3-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(185b) (103 mg, 0.21 mmol, 54% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) (mixture of two rotamers) δ 8.89 (t, J=5.8 Hz and, 8.49 (t,J=5.9 Hz) (2t, 1H), 8.22-8.13 (m, 1H), 7.74-7.64 (m, 1H), 7.63-7.00 (m,7H), 5.81-5.29 (m, 2H), 4.97-4.74 (m, 1H), 4.47 (d, J=5.6 Hz) and 4.31(d, J=5.9 Hz) (2d, 2H), 4.25 (s) and 4.00-3.43 (m) (s & m, 6H),2.42-1.54 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.27, −121.73; MS(ES+): 488.5 (M+1); MS (ES−): 486.5 (M−1).

Preparation of(R)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(tetrahydrofuran-3-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(186b) Step-1: Preparation of(R)—N-(3-chloro-2-fluorobenzyl)-2-((tetrahydrofuran-3-yl)-amino)acetamide(186a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (339 mg,1.44 mmol) with (R)-tetrahydrofuran-3-amine (250 mg, 2.87 mmol)according to the procedure reported in step-2 of Scheme 35 gave afterworkup and purification by flash column chromatography [silica (12 g),eluting with EtOAc/MeOH (9:1) in hexane 0 to 60%](R)—N-(3-chloro-2-fluorobenzyl)-2-((tetrahydrofuran-3-yl)amino)acetamide(186a) (109 mg, 0.38 mmol, 27%) as a colorless oil; MS (ES+): 287.4(M+1), 309.3 (M+Na); MS (ES−): 285.3

Step-2: Preparation of(R)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(tetrahydrofuran-3-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide (186b)

Reaction of(R)—N-(3-chloro-2-fluorobenzyl)-2-((tetrahydrofuran-3-yl)amino)acetamide(186a) (109 mg, 0.38 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (92 mg, 0.42 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with DMA80 in DCM 0 to 60%](R)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(tetrahydrofuran-3-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(186b) (23 mg, 0.047 mmol, 12% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.95-8.43 (m, 1H), 8.23-8.13 (m, 1H), 7.74-7.64 (m, 1H),7.63-6.95 (m, 7H), 5.76-5.54 (m) and 5.40 (s) (2H), 5.00-4.73 (m, 1H),4.47 (d, J=5.5 Hz) and 4.32 (d, J=5.9 Hz) (2d, 2H), 4.25 (s) and4.02-3.51 (m) (6H), 2.16-1.61 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.28, −121.74; MS (ES+): 488.5 (M+1); MS (ES−): 486.5 (M−1).

Preparation of2-(3-acetyl-5-(pyridin-3-ylamino)-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(187c) Step-1: Preparation of tert-butyl2-(3-acetyl-5-(pyridin-3-ylamino)-1H-indazol-1-yl)acetate (187a)

Reaction of tert-butyl 2-(3-acetyl-5-bromo-1H-indazol-1-yl)acetate(156d) (935 mg, 2.65 mmol) with pyridin-3-amine (0.498 g, 5.29 mmol),using potassium carbonate (732 mg, 5.29 mmol),di-tert-butyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine (135 mg, 0.32mmol), Pd₂(dba)₃ (145 mg, 0.16 mmol) according to the procedure reportedin step-1 of Scheme 97 gave after workup and purification by flashcolumn chromatography [silica gel (40 g), eluting with DMA80 in DCM 0 to50] tert-butyl 2-(3-acetyl-5-(pyridin-3-ylamino)-1H-indazol-1-yl)acetate(187a) (722 mg, 1.97 mmol, 74% yield) as a yellow solid; ¹H NMR (300MHz, DMSO-d₆) δ 8.54 (s, 1H), 8.37 (d, J=2.8 Hz, 1H), 8.05 (dd, J=4.6,1.4 Hz, 1H), 7.88 (d, J=2.1 Hz, 1H), 7.68 (d, J=9.0 Hz, 1H), 7.56-7.41(m, 1H), 7.38-7.22 (m, 2H), 5.41 (s, 2H), 2.59 (s, 3H), 1.44 (s, 9H); MS(ES+): 367.5 (M+1), 389.5 (M+Na); MS (ES−): 365.4 (M−1).

Step-2: Preparation of2-(3-acetyl-5-(pyridin-3-ylamino)-1H-indazol-1-yl)acetic acid (187b)

Reaction of tert-butyl2-(3-acetyl-5-(pyridin-3-ylamino)-1H-indazol-1-yl)acetate (187a) (115mg, 0.31 mmol) with TFA (0.73 mL, 9.42 mmol) according to the procedurereported in step-2 of Scheme 2 gave after workup and trituration withhexane (10 mL) 2-(3-acetyl-5-(pyridin-3-ylamino)-1H-indazol-1-yl)aceticacid (187b) (129 mg, 0.3 mmol, 97% yield) as a yellow solid in the formof TFA adduct; ¹H NMR (300 MHz, DMSO-d₆) δ 13.44 (bs, 1H, D₂Oexchangeable), 9.34 (s, 1H, D₂O exchangeable), 8.41 (s, 1H), 8.24 (d,J=5.3 Hz, 1H), 8.05-7.92 (m, 2H), 7.85 (d, J=9.0 Hz, 1H), 7.78 (dd,J=8.7, 5.2 Hz, 1H), 7.44 (dd, J=9.0, 2.1 Hz, 1H), 5.47 (s, 2H), 2.61 (s,3H); MS (ES+): 311.4 (M+1); MS (ES−): 619.5 (2M−1).

Step-3: Preparation of2-(3-acetyl-5-(pyridin-3-ylamino)-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(187c)

Reaction of 2-(3-acetyl-5-(pyridin-3-ylamino)-1H-indazol-1-yl)aceticacid (187b) (234 mg, 0.754 mmol) withN-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide (19c) (234 mg,0.91 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column [silica gel (12 g),eluting with DMA-80 in DCM 0-100%] 2-(3-acetyl-5-(pyridin-3-ylamino)-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(187c) (38 mg, 0.069 mmol, 9% yield) as a yellow solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.84 (t, J=5.8 Hz) and 8.42-8.29 (m) (t & m, 2H), 8.52 (s,1H), 8.10-8.00 (m, 1H), 7.88 (d, J=2.0 Hz, 1H), 7.63-6.99 (m, 6H), 5.66& 5.49 (2s, 2H), 4.66-4.52 & 4.30-4.22 (2m, 1H), 4.47 (d, J=5.6 Hz) and4.33 (d, J=5.9 Hz) (2d, 2H), 4.18 & 3.86 (2s, 2H), 2.58 (s, 3H), 1.25(d, J=6.5 Hz) & 1.01 (d, J=6.8 Hz) (2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆)δ −121.21, −121.72; MS (ES+): 573.5, 575.5 (M+Na); MS (ES−): 549.4(M−1);

Preparation of2-(3-acetyl-5-(pyridin-3-ylamino)-1H-indazol-1-yl)-N-(2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)-N-isopropylacetamide(188a)

Reaction of 2-(3-acetyl-5-(pyridin-3-ylamino)-1H-indazol-1-yl)aceticacid (187b) (210 mg, 0.68 mmol) withN-(6-bromopyridin-2-yl)-2-(isopropylamino)acetamide (28b) (221 mg, 0.81mmol) according to the procedure reported in step-3 of Scheme 2 gaveafter workup and purification by flash column [silica gel (24 g),eluting with DMA-80 in DCM 0-100%]2-(3-acetyl-5-(pyridin-3-ylamino)-1H-indazol-1-yl)-N-(2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)-N-isopropylacetamide(188a) (139 mg, 0.25 mmol, 36% yield) as a light green solid as amixture of two rotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 11.21 & 10.82 (2s,1H, D₂O exchangeable), 8.53 & 8.51 (2s, 1H), 8.36 (t, J=3.3 Hz, 1H),8.23-7.97 (m, 2H), 7.88 (d, J=2.0 Hz) & 7.86 (d, J=2.1 Hz) (2d, 1H),7.81 (t, J=8.0 Hz) & 7.70 (t, J=8.0 Hz) (2t, 1H), 7.61 (d, J=3.4 Hz) &7.58 (d, J=3.4 Hz) (2d, 1H), 7.50-7.21 (m, 4H), 5.70 & 5.51 (2s, 2H),4.71-4.57 & 4.38-4.26 (2m, 1H), 4.43 & 4.05 (2s, 2H), 2.59 & 2.58 (2s,3H), 1.26 (d, J=6.4 Hz) &, 1.05 (d, J=6.8 Hz) (2d, 6H); MS (ES+): 564.5& 566.5 (M+1), 586.5 & 588.5 (M+Na); MS (ES−): 562.4 & 564.4 (M−1).

Preparation of3-acetyl-N-benzyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indole-5-carboxamide(189a)

Reaction of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indole-5-carboxylicacid (129c) (50 mg, 0.1 mmol) with phenylmethanamine (0.016 mL, 0.15mmol) according to the procedure reported in step-3 of Scheme 2 gaveafter workup and purification by flash column [silica gel (4 g), elutingwith CHCl₃/MeOH (1:0 to 19:1)]3-acetyl-N-benzyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indole-5-carboxamide(189a) (47 mg, 80%) as a light brown solid; ¹H NMR (300 MHz, DMSO-d₆) δ9.09-8.79 (m, 1H), 8.77-8.73 (m, 1H), 8.35 and 8.31 (2s, 1H), 7.82-6.93(m, 11H), 5.40 and 5.21 (2s, 2H), 4.62-4.21 (m, 5H), 4.19 and 3.85 (2s,2H), 2.46 and 2.45 (2s, 3H), 1.26 (d, J=6.5 Hz) and 1.00 (d, J=6.8 Hz(2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.19, −121.80; MS (ES−): 589.9& 591.6 (M−1), 625.5 & 627.6 (M+Cl).

Preparation of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-N-(cyclopropylmethyl)-1H-indole-5-carboxamide(190a)

Reaction of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indole-5-carboxylicacid (129c) (50 mg, 0.1 mmol) with cyclopropylmethanamine (0.013 mL,0.149 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column [silica gel (4 g),eluting with CHCl₃/MeOH (1:0 to 19:1)]3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-N-(cyclopropylmethyl)-1H-indole-5-carboxamide(190a) (39 mg, 71%) as an off-white solid; ¹H NMR (300 MHz, DMSO-d₆)(mixture of two rotamers) δ 8.89-8.48 (m, 2H), 8.34 and 8.30 (2s, 1H),7.79-6.91 (m, 6H), 5.39 and 5.20 (2s, 2H), 4.65-4.51 and 4.29-4.20 (2m,1H), 4.48 (d, J=5.5 Hz) and 4.33 (d, J=5.8 Hz) (2d, 2H), 4.19 and 3.85(2s, 2H), 3.16 (t, J=6.1 Hz, 2H), 2.46 and 2.45 (2s, 3H), 1.26 (d, J=6.5Hz) and 1.00 (d, J=6.8 Hz) (2d, 6H), 1.12-1.01 (m, 1H), 0.48-0.38 (m,2H), 0.29-0.19 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.19, −121.79;MS (ES+): 555.6 (M+1) and 577.6 (M+Na), MS (ES−): 589.6 & 591.5 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-N5-(pyridin-2-ylmethyl)-1H-indazole-3,5-dicarboxamide(191a)

Reaction of3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (144a) (50 mg, 0.1 mmol) with pyridin-2-ylmethanamine (0.015 mL,0.15 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column chromatography[silica (4 g), eluting with MeOH in DCM (1:0 to 9:1)]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-N5-(pyridin-2-ylmethyl)-1H-indazole-3,5-dicarboxamide(191a) (27 mg, 46%) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) (mixtureof two rotamers) δ 9.28 (t, J=5.8 Hz, 1H), 8.84 (t, J=5.7 Hz) and 8.37(t, J=5.9 Hz)(2t, 1H), 8.81-8.78 (m, 1H), 8.55-8.50 (m, 1H), 8.01-7.90(m, 1H), 7.86-7.73 (m, 2H), 7.69 (d, J=8.9 Hz) and 7.62 (d, J=8.8 Hz)(2d, 1H), 7.55-6.94 (m, 6H), 5.64 and 5.50 (2s, 2H), 4.60 (d, J=5.8 Hz,2H), 4.58-4.49 and 4.29-4.21 (2m, 1H), 4.46 (d, J=5.6 Hz) and 4.31 (d,J=5.8 Hz) (2d, 2H), 4.19 and 3.84 (2s, 2H), 1.23 (d, J=6.3 Hz) and 0.99(d, J=6.8 Hz) (2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.22, −121.73;MS (ES+): 594.6 & 596.6 (M+1); 628.5 & 630.6 (M+Na).

Preparation of2-(3-acetyl-5-(3,3-difluoropiperidine-1-carbonyl)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(192a)

Reaction of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indole-5-carboxylicacid (165b) (50 mg, 0.1 mmol) with 3,3-difluoropiperidine hydrochloride(24 mg, 0.15 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup and purification by flash columnchromatography [silica (4 g), eluting with MeOH in DCM (1:0 to 19:1)]2-(3-acetyl-5-(3,3-difluoropiperidine-1-carbonyl)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(192a) (39 mg, 65%) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 8.47(t, J=5.8 Hz, 1H), 8.39 (s, 1H), 8.22 (d, J=1.6 Hz, 1H), 7.54 (d, J=8.5Hz, 1H), 7.45 (td, J=7.7, 1.7 Hz, 1H), 7.28-7.16 (m, 2H), 7.09 (td,J=7.9, 1.0 Hz, 1H), 5.48 (s, 2H), 4.34 (d, J=5.7 Hz, 2H), 4.00 (s, 2H),3.96-3.42 (m, 4H), 3.17-3.04 (m, 1H), 2.44 (s, 3H), 2.20-1.98 (m, 2H),1.70 (bs, 2H), 1.05-0.82 (m, 4H); MS (ES+): 603.6 (M+1); MS (ES−): 601.6(M−1), 637.6, 639.6 (M+Cl).

Preparation of2-(3-acetyl-5-(2-(dimethylamino)pyrimidin-5-yl)-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(193a)

Reaction of2-(3-acetyl-5-bromo-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(156f) (150 mg, 0.28 mmol) with 2-(dimethylamino)pyrimidin-5-ylboronicacid (47 mg, 0.28 mmol) according the procedure reported in Scheme 100gave after workup and purification by flash column chromatography[silica gel (12 g), eluting with CMA80 in CHCl₃ 0 to 20%]2-(3-acetyl-5-(2-(dimethylamino)pyrimidin-5-yl)-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(193a) (50 mg, 0.093 mmol, 33% yield) as a white solid as a mixture oftwo rotamers; ¹H NMR (300 MHz, DMSO-d₆) (mixture of two rotamers) δ 8.84and 8.36 (2t, J=5.8 Hz, 1H), 8.71 (s, 2H), 8.31-8.26 (m, 1H), 7.82-6.92(m, 5H), 5.73 and 5.55 (2s, 2H), 4.64-4.51 and 4.30-4.22 (2m, 1H), 4.48and 4.32 (2d, J=5.6 Hz, 2H), 4.19 and 3.85 (2s, 2H), 3.199 and 3.19 (2s,6H), 2.63 (s, 3H), 1.25 and 1.00 (2d, J=6.7 Hz, 6H); ¹⁹F NMR (282 MHz,DMSO-d₆) (mixture of two rotamers) δ −121.20, −121.74; MS (ES+): 580.6(M+1), MS (ES−): 614.5 (M+Cl).

Preparation of2-(3-acetyl-5-(pyrimidin-5-yl)-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(194a)

Reaction of2-(3-acetyl-5-bromo-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(156f) (150 mg, 0.28 mmol) with pyrimidin-5ylboronic acid (0.035 g, 0.28mmol) according the procedure reported in Scheme 100 gave after workupand purification by flash column chromatography [silica gel (12 g),eluting with CMA80 in CHCl₃ 0 to 20%]2-(3-acetyl-5-(pyrimidin-5-yl)-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(194a) (98 mg, 0.18 mmol, 65% yield) as a white solid as a mixture oftwo rotamers; ¹H NMR (300 MHz, DMSO-d₆) (a mixture of two rotamers) δ9.228 and 9.22 (2s, 1H), 9.187 and 9.18 (2s, 2H), 8.85 and 8.36 (2t,J=5.6 Hz, 1H), 8.51-8.44 (m, 1H), 7.97-7.75 (m, 2H), 7.57-6.96 (m, 3H),5.77 and 5.59 (2s, 2H), 4.65-4.52 and 4.30-4.17 (2m, 1H), 4.48 and 4.32(2d, J=5.8 Hz, 2H), 4.20 and 3.86 (2s, 2H), 2.65 (s, 3H), 1.27 and 1.01(2d, J=6.8 Hz, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) (mixture of two rotamers)δ −121.20, −121.74; MS (ES+): 537.5 (M+1), 559.6 (M+Na); MS (ES−): 571.5(M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((3-hydroxyoxetan-3-yl)methyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(195b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-((2-(3-hydroxyoxetan-3-yl)ethyl)amino)acetamide(195a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (410 mg,1.74 mmol) with 3-(aminomethyl)oxetan-3-ol (269 mg, 2.61 mmol) accordingto the procedure reported in step-2 of Scheme 35 gave after workupN-(3-chloro-2-fluorobenzyl)-2-((3-hydroxyoxetan-3-yl)methylamino)acetamide(195a) (250 mg, 0.83 mmol, 48%) as an oil which was used in the nextstep without further purification; MS (ES+) 303.4 (M+1); (ES−) 301.3(M−1).

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((3-hydroxyoxetan-3-yl)methyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(195b)

Reaction of N-(3-chloro-2-fluorobenzyl)-2-((2-(3-hydroxyoxetan-3-yl)ethyl)amino)acetamide (195a) (250 mg, 0.83 mmol) with2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e) (181 mg, 0.83 mmol)according to the procedure reported in step-3 of Scheme 2 gave afterworkup and purification by flash column chromatography [silica (12 g),eluting with MeOH in DCM 0 to 50%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxo ethyl)((3-hydroxyoxetan-3-yl)methyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide (195b)(85 mg, 0.17 mmol, 20% yield) as a white solid as a mixture as arotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 8.81 (t, J=5.7 Hz) & 8.58 (t,J=5.8 Hz) (2t, 1H, D₂O exchangeable), 8.21-8.16 (m, 1H), 7.74 & 7.71(2s, 1H), 7.59-7.02 (m, 7H), 6.52 & 6.05 (2s, 1H, D₂O exchangeable),5.63 & 5.45 (2s, 2H), 4.61-4.29 (m, 8H), 4.04 & 3.94 (2s, 2H); ¹⁹F NMR(282 MHz, DMSO-d₆) δ −121.39, −121.56; MS (ES+): 526.5 (M+Na); MS (ES−):502.4 (M−1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-N5-(pyridin-3-ylmethyl)-1H-indazole-3,5-dicarboxamide(196a)

Reaction of3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (144a) (50 mg, 0.1 mmol) with pyridin-3-ylmethanamine (0.015 mL,0.15 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column chromatography[silica (4 g), eluting with MeOH in DCM (1:0 to 9:1)]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-N5-(pyridin-3-ylmethyl)-1H-indazole-3,5-dicarboxamide(196a) (32 mg, 54%) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) (mixtureof two rotamers) δ 9.30-9.21 (m, 1H), 8.83 (t, J=5.7 Hz) and 8.36 (t,J=6.0 Hz) (2t, 1H) 8.78-8.74 (m, 1H), 8.61-8.55 (m, 1H), 8.46 (dt,J=4.8, 1.6 Hz, 1H), 7.98-6.94 (m, 9H), 5.63 and 5.49 (2s, 2H), 4.60-4.45and 4.30-4.20 (2m, 1H), 4.53 (d, J=6.0 Hz, 2H), 4.46 (d, J=5.6 Hz) and4.31 (d, J=5.9 Hz) (2d, 2H), 4.18 and 3.83 (2s, 2H), 1.23 (d, J=6.3 Hz)and 0.99 (d, J=6.8 Hz) (2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.22,−121.73; MS (ES+): 594.6 (M+1); MS (ES−): 628.6 & 630.6 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(3,3-difluoropiperidine-1-carbonyl)-1H-indazole-3-carboxamide(197a)

Reaction of3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (144a) (50 mg, 0.1 mmol) with 3,3-difluoropiperidine hydrochloride(24 mg, 0.15 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup and purification by flash columnchromatography [silica (8 g), eluting with MeOH in DCM (1:0 to 19:1)]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(3,3-difluoropiperidine-1-carbonyl)-1H-indazole-3-carboxamide(197a) (43 mg, 71%) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 8.84(t, J=5.8 Hz) and 8.37 (t, J=5.9 Hz) (2t, 1H), 8.21 (bs, 1H), 7.82 and7.80 (2s, 1H), 7.74-7.58 (m, 1H), 7.55-6.96 (m, 5H), 5.64 and 5.50 (2s,2H), 4.63-4.49 and 4.29-4.212 (m, 1H), 4.46 (d, J=5.6 Hz) and 4.31 (d,J=5.8 Hz) (2d, 2H), 4.18 and 3.84 (2s, 2H), 4.10-3.20 (m, 4H), 2.21-2.02(m, 2H), 1.71 (bs, 2H), 1.24 (d, J=6.4 Hz) and 0.99 (d, J=6.8 Hz) (2d,6H); MS (ES+): 607.6 & 609.6 (M+1).

Preparation of methyl3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylate(198a)

Reaction of 2-(3-carbamoyl-5-(methoxycarbonyl)-1H-indazol-1-yl)aceticacid, TFA adduct (132f) (4.38 g, 11.19 mmol) withN-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide (19c) (3.22 g,12.54 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column [silica (40 g),eluting with DMA80 in DCM 0 to 30%] methyl3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylate(198a) (4.23 g, 8.20 mmol, 73% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.91-8.84 (m, 1H), 8.50 (t, J=5.8 Hz, 1H), 7.97 (dd, J=8.9,1.6 Hz, 1H), 7.90 (s, 1H), 7.80-7.73 (m, 1H), 7.60-7.53 (m, 1H),7.50-7.41 (m, 1H), 7.26-7.17 (m, 1H), 7.15-7.05 (m, 1H), 5.72 (s, 2H),4.33 (d, J=5.7 Hz, 2H), 3.98 (s, 2H), 3.90 (s, 3H), 3.14-3.01 (m, 1H),1.06-0.97 (m, 2H), 0.96-0.86 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.56; MS (ES+) 516.4 (M+1); (ES−) 514.3 (M−1).

Preparation of3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (199a)

Reaction of methyl3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylate(198a) (4.17 g, 8.08 mmol) in THF (50 mL) and water (50 mL) using asolution of lithium hydroxide hydrate (2.37 g, 56.6 mmol) in water (20mL) according to the procedure reported in step-2 of Scheme 29 gaveafter workup3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (199a) (4.06 g, 8.09 mmol, 100% yield) as a white solid, which wasused in the next step without further purification; ¹H NMR (300 MHz,DMSO-d₆) δ 12.84 (s, 1H), 8.89-8.81 (m, 1H), 8.56 (t, J=5.9 Hz, 1H),8.01-7.91 (m, 1H), 7.87 (s, 1H), 7.79-7.70 (m, 1H), 7.53 (s, 1H),7.50-7.41 (m, 1H), 7.28-7.19 (m, 1H), 7.14-7.05 (m, 1H), 5.72 (s, 2H),4.33 (d, J=5.7 Hz, 2H), 3.99 (s, 2H), 3.12-2.99 (m, 1H), 1.11-0.98 (m,2H), 0.98-0.84 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.58; MS (ES+):502.5 (M+1); (ES−): 501.5 (M−1).

Preparation ofN-benzyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-3-cyano-1H-indole-5-carboxamide(200i) Step-1: Preparation of methyl 3-formyl-1H-indole-5-carboxylate(200b)

To a solution of methyl 1H-indole-5-carboxylate (200a) (4 g, 22.83 mmol)in DMF (36 mL) cooled to 0° C. was added phosphoryl trichloride (2.87mL, 31.1 mmol) and stirred at RT for 2 h. The reaction mixture wasquenched with water (130 mL) refluxed for 15 min, cooled to RT and solidobtained was collected by filtration, washed with water, hexanes, driedunder vacuum to give methyl 3-formyl-1H-indole-5-carboxylate (200b)(4.38 g, 94%) as a light brown solid; ¹H NMR (300 MHz, DMSO-d₆) δ 12.45(s, 1H), 9.98 (s, 1H), 8.77 (dd, J=1.7, 0.7 Hz, 1H), 8.45 (s, 1H), 7.88(dd, J=8.6, 1.8 Hz, 1H), 7.61 (dd, J=8.6, 0.7 Hz, 1H), 3.87 (s, 3H); MS(ES+): 204.2 (M+1).

Step-2: Preparation of methyl 3-cyano-1H-indole-5-carboxylate (200c)

To a solution of methyl 3-formyl-1H-indole-5-carboxylate (200b) (1.02 g,5 mmol), hydroxylamine hydrochloride (556 mg, 8 mmol), and sodiumacetate (451 mg, 5.5 mmol) in acetic acid (7.5 mL) was added aceticanhydride (1.0 mL, 10.6 mmol) and heated at reflux for 6.5 h. Thereaction mixture was diluted with ice-water, solid separated wascollected by filtration, washed with water, dried under vacuum to givemethyl 3-cyano-1H-indole-5-carboxylate (200c) (856 mg, 86%) as a brownsolid; ¹H NMR (300 MHz, DMSO-d₆) δ 12.57 (s, 1H), 8.42 (s, 1H), 8.25(dd, J=1.7, 0.7 Hz, 1H), 7.89 (dd, J=8.6, 1.6 Hz, 1H), 7.66 (dd, J=8.6,0.7 Hz, 1H), 3.88 (s, 3H); MS (ES+): 223.3 (M+Na).

Step-3: Preparation of methyl1-(2-(tert-butoxy)-2-oxoethyl)-3-cyano-1H-indole-5-carboxylate (200d)

Reaction of methyl 3-cyano-1H-indole-5-carboxylate (200c) (800 mg, 4.0mmol) with tert-butyl 2-bromoacetate (0.89 mL, 5.99 mmol) according tothe procedure reported in step-1 of Scheme 56 gave after workup methyl1-(2-(tert-butoxy)-2-oxoethyl)-3-cyano-1H-indole-5-carboxylate (200d)(1.29 g, 4 mmol) which was used as such for next step; MS (ES⁺): 337.4(M+Na).

Step-4: Preparation of2-(3-cyano-5-(methoxycarbonyl)-1H-indol-1-yl)acetic acid (200e)

Reaction of methyl1-(2-(tert-butoxy)-2-oxoethyl)-3-cyano-1H-indole-5-carboxylate (200d)from above (1.27 g) with TFA (4.55 mL, 59.1 mmol) according to theprocedure reported in step-2 of Scheme 2 gave after workup2-(3-cyano-5-(methoxycarbonyl)-1H-indol-1-yl)acetic acid (200e) whichwas used as such in next step; MS (ES+): 281.3 (M+Na).

Step-5: Preparation of methyl1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-3-cyano-1H-indole-5-carboxylate(200f)

Reaction of 2-(3-cyano-5-(methoxycarbonyl)-1H-indol-1-yl)acetic acid(200e) (crude from above, 4 mmol) withN-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide (10b) (1.21 g,4.73 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column [silica (12 g),eluting with hexanes/10% MeOH in EtOAc (1:0 to 1:1)] methyl1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-3-cyano-1H-indole-5-carboxylate(200f) (446 mg, 23% yield for three steps) as an off white solid; ¹H NMR(300 MHz, DMSO-d₆) δ 8.46 (t, J=5.8 Hz, 1H), 8.34 (s, 1H), 8.26-8.23 (m,1H), 7.87 (dd, J=8.8, 1.6 Hz, 1H), 7.72-7.66 (m, 1H), 7.50-7.41 (m, 1H),7.25-7.18 (m, 1H), 7.12-7.04 (m, 1H), 5.53 (s, 2H), 4.34 (d, J=5.7 Hz,2H), 3.98 (s, 2H), 3.89 (s, 3H), 3.18-3.00 (m, 1H), 1.03-0.85 (m, 4H);¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.57; MS (ES+): 497.5 (M+1); MS (ES−):495.5 & 497.5 (M−1).

Step-6: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-3-cyano-1H-indole-5-carboxylicacid (200g)

Reaction of methyl1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-3-cyano-1H-indole-5-carboxylate(200f) (429 mg, 0.863 mmol) in MeOH (30 mL) using 2 N aqueous NaOH (2.59mL, 5.18 mmol) according to the procedure reported in step-4 of scheme43 gave after workup1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-3-cyano-1H-indole-5-carboxylicacid (200g) (371 mg, 89% yield) as an off-white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.46 (t, J=5.8 Hz, 1H), 8.31 (s, 1H), 8.24-8.21 (m, 1H), 7.86(dd, J=8.7, 1.6 Hz, 1H), 7.67 (d, J=8.7 Hz, 1H), 7.45 (td, J=7.6, 1.8Hz, 1H), 7.27-7.17 (m, 1H), 7.09 (td, J=7.9, 1.0 Hz, 1H), 5.52 (s, 2H),4.34 (d, J=5.7 Hz, 2H), 3.98 (s, 2H), 3.18-3.00 (m, 1H), 1.09-0.79 (m,4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.56; MS (ES−): 517.4 & 519.5(M+Cl).

Step-7: Preparation ofN-benzyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-3-cyano-1H-indole-5-carboxamide(200h)

Reaction of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-3-cyano-1H-indole-5-carboxylicacid (200g) (100 mg, 0.21 mmol) with phenylmethanamine (0.034 mL, 0.31mmol) according to the procedure reported in step-3 of Scheme 2 gaveafter workup and purification by flash column [silica (12 g), elutingDCM/MeOH (1:0 to 19:1)]N-benzyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-3-cyano-1H-indole-5-carboxamide(200h) as a light brown gum; MS (ES−): 606.6 (M+Cl).

Step-8: Preparation ofN-benzyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-3-cyano-1H-indole-5-carboxamide(200i)

Reaction ofN-benzyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-3-cyano-1H-indole-5-carboxamide(200h) (132 mg) in ethanol (4 mL) using conc. NH₄OH (1.5 mL) and H₂O₂(aq. 35%, 0.066 mL, 0.74 mmol) according to the procedure reported inScheme 65 gave after workup and purification by flash columnchromatography [silica (4 g), eluting with DCM/MeOH (1:0 to 19:1)]N-benzyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-3-cyano-1H-indole-5-carboxamide(200i) (56 mg, 51% for two steps) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.99 (t, J=6.0 Hz, 1H), 8.71 (d, J=1.8 Hz, 1H), 8.47 (t,J=5.8 Hz, 1H), 8.01 (s, 1H), 7.71 (dd, J=8.7, 1.7 Hz, 1H), 7.54-6.87 (m,11H), 5.42 (s, 2H), 4.50 (d, J=6.0 Hz, 2H), 4.34 (d, J=5.7 Hz, 2H), 3.99(s, 2H), 3.15-3.02 (m, 1H), 1.06-0.82 (m, 4H); ¹⁹F NMR (282 MHz,DMSO-d₆) δ −121.61; MS (ES+): 590.7 & 592.6 (M+1); MS (ES−): 624.5 &626.6 (M+Cl).

Preparation of3-acetyl-N-benzyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indole-6-carboxamide(201d) Step-1: Preparation of methyl3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indole-6-carboxylate(201b)

Reaction of 2-(3-acetyl-6-(methoxycarbonyl)-1H-indol-1-yl)acetic acid(201a) TFA adduct (10.77 g, 27.7 mmol, Prepared according to theprocedure reported by Altmann, Eva et al; in PCT Int. Appl., WO2012/093101) withN-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide (10b) (7.10 g,27.7 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and trituration of crude with EtOAc, methyl3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indole-6-carboxylate(201b) (8.17 g, 57%) as an off-white; ¹H NMR (300 MHz, DMSO-d₆) δ8.55-8.43 (m, 2H), 8.27 (dd, J=8.4, 0.7 Hz, 1H), 8.15 (dd, J=1.5, 0.7Hz, 1H), 7.82 (dd, J=8.4, 1.4 Hz, 1H), 7.48-7.36 (m, 1H), 7.26-7.16 (m,1H), 7.04 (td, J=7.9, 1.1 Hz, 1H), 5.57 (s, 2H), 4.35 (d, J=5.8 Hz, 2H),3.99 (s, 2H), 3.82 (s, 3H), 3.20-3.05 (m, 1H), 2.45 (s, 3H), 1.08-0.80(m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.72; MS (ES+): 514.5 & 516.5(M+1).

Step-2: Preparation of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indole-6-carboxylicacid (201c)

Reaction of methyl3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indole-6-carboxylate(201b) (8 g, 15.57 mmol) in THF (100 mL) and MeOH (100 mL) using asolution of lithium hydroxide hydrate (4 g, 93 mmol) in water (100 mL)according to the procedure reported in step-2 of Scheme 129 gave afterworkup3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indole-6-carboxylicacid (201c) (8.012 g) as a light brown solid. ¹H NMR (300 MHz, DMSO-d₆)δ 12.80 (s, 1H), 8.53-8.41 (m, 2H), 8.24 (dd, J=8.4, 0.6 Hz, 1H),8.15-8.11 (m, 1H), 7.81 (dd, J=8.3, 1.4 Hz, 1H), 7.45 (td, J=7.7, 7.2,1.7 Hz, 1H), 7.27-7.17 (m, 1H), 7.08 (td, J=7.9, 1.0 Hz, 1H), 5.55 (s,2H), 4.34 (d, J=5.8 Hz, 2H), 3.99 (s, 2H), 3.20-3.06 (m, 1H), 2.45 (s,3H), 1.08-0.82 (m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.66; MS (ES+):522.5 & 524.5 (M+Na).

Step-3: Preparation of3-acetyl-N-benzyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indole-6-carboxamide(201d)

Reaction of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indole-6-carboxylicacid (201c) (50 mg, 0.1 mmol) with phenylmethanamine (0.017 mL, 0.15mmol) according to the procedure reported in step-3 of Scheme 2 gaveafter workup and purification by flash column [silica (4 g), elutingDCM/MeOH (1:0 to 19:1)]3-acetyl-N-benzyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indole-6-carboxamide(201d) (31 mg, 53%) as a light yellow solid. ¹H NMR (300 MHz, DMSO-d₆) δ8.96 (t, J=6.0 Hz, 1H), 8.54 (t, J=5.8 Hz, 1H), 8.42 (s, 1H), 8.22 (d,J=8.3 Hz, 1H), 8.02 (s, 1H), 7.78 (dd, J=8.4, 1.4 Hz, 1H), 7.47-7.39 (m,1H), 7.34-7.15 (m, 6H), 7.04 (t, J=7.9 Hz, 1H), 5.52 (s, 2H), 4.50 (d,J=5.9 Hz, 2H), 4.30 (d, J=5.8 Hz, 2H), 4.01 (s, 2H), 3.22-3.02 (m, 1H),2.45 (s, 3H), 1.05-0.80 (m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.58;MS (ES+): 589.6 (M+1); MS (ES−): 623.5 & 625.5 (M+Cl).

Preparation of2-(3-acetyl-6-bromo-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(202e) Step-1: Preparation of 1-(6-bromo-1H-indol-3-yl)ethanone (202b)

To a solution of 6-bromo-1H-indole (202a) (5 g, 25.5 mmol) in toluene(80 mL) at 0° C. under inert atmosphere was added acetyl chloride (2.72mL, 38.3 mmol), stirred for 10 mins followed by dropwise addition ofTin(IV) chloride (4.49 mL, 38.3 mmol) in toluene (20 mL). The reactionmixture was stirred at 0° C. for 3h in ice-water bath and the pink finesuspension was poured into a bi-phasic layer of aqueous saturated NaHCO₃(600 mL) and EtOAc (400 mL). The mixture was stirred vigorously for 15min and filtered over Celite pad to remove inorganic impurities. Theorganic layer was separated washed with brine, dried, filtered andconcentrated in vacuum to afford 1-(6-bromo-1H-indol-3-yl)ethanone(202b) (4.15 g, 17.43 mmol, 68% yield) as a white solid; ¹H NMR (300MHz, DMSO-d₆) δ 12.04 (s, 1H), 8.34 (d, J=1.6 Hz, 1H), 8.10 (dd, J=8.5,0.6 Hz, 1H), 7.65 (dd, J=1.8, 0.6 Hz, 1H), 7.31 (dd, J=8.5, 1.8 Hz, 1H),2.44 (s, 3H); MS (ES+): 238.2, 240.2 (M+2); MS (ES−): 236.1, 238.1(M−2).

Step-2: Preparation of tert-butyl2-(3-acetyl-6-bromo-1H-indol-1-yl)acetate (202c)

Reaction of 1-(6-bromo-1H-indol-3-yl)ethanone (202b) (4 g, 16.8 mmol)with tert-butyl 2-bromoacetate (4.97 mL, 33.6 mmol) according to theprocedure reported in step-1 of Scheme 56 gave after workup andtrituration of crude with 20% EtOAc-hexane (40 mL), tert-butyl2-(3-acetyl-6-bromo-1H-indol-1-yl)acetate (202c) (4.49 g, 12.75 mmol,76% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 8.34 (s, 1H),8.11 (dd, J=8.5, 0.5 Hz, 1H), 7.82 (dd, J=1.8, 0.5 Hz, 1H), 7.36 (dd,J=8.5, 1.7 Hz, 1H), 5.14 (s, 2H), 2.43 (s, 3H), 1.44 (s, 9H); MS (ES+):352.3, 354.3 (M+2), MS (ES−): 386.2, 388.2 (M+Cl).

Step-3: Preparation of 2-(3-acetyl-6-bromo-1H-indol-1-yl)acetic acid(202d)

Reaction of tert-butyl 2-(3-acetyl-6-bromo-1H-indol-1-yl)acetate (202c)(1.5 g, 4.26 mmol) with TFA (6.56 mL, 85 mmol) according to theprocedure reported in step-2 of Scheme 2 gave after workup andtrituration of crude with 20% EtOAc-hexane (10 mL),2-(3-acetyl-6-bromo-1H-indol-1-yl)acetic acid (202d) TFA adduct (1.25 g,4.22 mmol, 99% yield) as an off-white solid; III NMR (300 MHz, DMSO-d₆)δ 13.26 (s, 1H, D₂O exchangeable), 8.36 (s, 1H), 8.10 (dd, J=8.5, 0.5Hz, 1H), 7.86 (dd, J=1.8, 0.5 Hz, 1H), 7.36 (dd, J=8.5, 1.7 Hz, 1H),5.15 (s, 2H), 2.43 (s, 3H); MS (ES+): 296.2, 298.3 (M+2); MS (ES−);294.2, 296.2 (M−2).

Step-4: Preparation of2-(3-acetyl-6-bromo-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(202e)

Reaction of 2-(3-acetyl-6-bromo-1H-indol-1-yl)acetic acid (202d) (600mg, 2.03 mmol) withN-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide (10b) (572 mg,2.23 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column [silica gel (24 g),eluting with DMA80-DCM 0 to 20%]2-(3-acetyl-6-bromo-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(202e) (0.78 g, 1.46 mmol, 72% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.47 (t, J=5.9 Hz, 1H), 8.30 (s, 1H), 8.10 (d, J=8.4 Hz, 1H),7.80 (d, J=1.7 Hz, 1H), 7.49-7.41 (m, 1H), 7.34 (dd, J=8.5, 1.7 Hz, 1H),7.28-7.19 (m, 1H), 7.09 (td, J=7.9, 1.1 Hz, 1H), 5.45 (s, 2H), 4.35 (d,J=5.8 Hz, 2H), 3.99 (s, 2H), 3.16-3.04 (m, 1H), 2.42 (s, 3H), 1.05-0.96(m, 2H), 0.95-0.85 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.66; MS(ES+) 534.4, 536.4 (M+1); MS (ES−): 570.3 (M+Cl).

Preparation of2-(3-acetyl-6-(pyrimidin-5-ylamino)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(203c) Step-1: Preparation of tert-butyl2-(3-acetyl-6-(pyrimidin-5-ylamino)-1H-indol-1-yl)acetate (203a)

Reaction of tert-butyl 2-(3-acetyl-6-bromo-1H-indol-1-yl)acetate (202c)(1.0 g, 2.84 mmol) with pyrimidin-5-amine (351 mg, 3.69 mmol) usingpotassium carbonate (785 mg, 5.68 mmol),di-tert-butyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine (169 mg, 0.4mmol), Pd₂(dba)₃ (182 mg, 0.2 mmol) according to the procedure reportedin step-1 of Scheme 97 gave after workup and purification by flashcolumn [silica gel (40 g), eluting with DMA80-DCM 0 to 20%] tert-butyl2-(3-acetyl-6-(pyrimidin-5-ylamino)-1H-indol-1-yl)acetate (203a) (72 mg,1.96 mmol, 69% yield) as an off-white solid; ¹H NMR (300 MHz, DMSO-d₆) δ8.60 (s, 1H), 8.59 (s, 1H), 8.55 (s, 2H), 8.21 (s, 1H), 8.09 (d, J=8.5Hz, 1H), 7.26 (d, J=1.9 Hz, 1H), 7.02 (dd, J=8.5, 1.9 Hz, 1H), 5.76 (s,1H), 5.10 (s, 2H), 2.42 (s, 3H), 1.43 (s, 9H); MS (ES+) 367.5 (M+1); MS(ES−): 365.4 (M−1).

Step-2: Preparation of2-(3-acetyl-6-(pyrimidin-5-ylamino)-1H-indol-1-yl)acetic acid (203b)

Reaction of tert-butyl2-(3-acetyl-6-(pyrimidin-5-ylamino)-1H-indol-1-yl)acetate (203a) (530mg, 1.45 mmol) with TFA (1.47 mL, 19.05 mmol) according to the procedurereported in step-2 of Scheme 2 gave after workup and trituration ofcrude with 30% EtOAc-hexane (10 mL),2-(3-acetyl-6-(pyrimidin-5-ylamino)-1H-indol-1-yl)acetic acid (203b) TFAadduct (470 mg, 1.11 mmol, 77% yield) as an orange solid; ¹H NMR (300MHz, DMSO-d₆) δ 8.60 (s, 1H), 8.55 (s, 2H), 8.23 (s, 1H), 8.09 (d, J=8.5Hz, 1H), 7.30 (d, J=1.9 Hz, 1H), 7.03 (dd, J=8.5, 2.0 Hz, 1H), 5.11 (s,2H), 2.42 (s, 3H).

Step-3: Preparation of2-(3-acetyl-6-(pyrimidin-5-ylamino)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(203c)

Reaction of N-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide(10b) (66 mg, 0.26 mmol) with2-(3-acetyl-6-(pyrimidin-5-ylamino)-1H-indol-1-yl)acetic acid (203b) (80mg, 0.26 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column chromatography[silica gel (12 g), eluting with DMA80-DCM 0 to 30%]2-(3-acetyl-6-(pyrimidin-5-ylamino)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(203c) (65 mg, 0.12 mmol, 46% yield) as an off-white solid; ¹H NMR (300MHz, DMSO-d₆) δ 8.56 (s, 1H), 8.53 (s, 1H), 8.51 (s, 2H), 8.44 (t, J=5.9Hz, 1H), 8.21 (s, 1H), 8.09 (d, J=8.5 Hz, 1H), 7.43 (td, J=7.7, 7.2, 1.7Hz, 1H), 7.27-7.17 (m, 2H), 7.14-6.98 (m, 2H), 5.41 (s, 2H), 4.31 (d,J=5.7 Hz, 2H), 3.98 (s, 2H), 3.12-2.98 (m, 1H), 2.41 (s, 3H), 1.01-0.94(m, 2H), 0.94-0.86 (m, 2H); 19F NMR (282 MHz, DMSO-d₆) δ −121.62; MS(ES+): 549.5 (M+1), 571.5 (M+Na), MS (ES−): 547.5 (M−1).

Preparation of2-(3-acetyl-6-(2-(dimethylamino)pyrimidin-5-yl)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(204a)

Reaction of2-(3-acetyl-6-bromo-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(202e) (150 mg, 0.28 mmol) with 2-(dimethylamino)pyrimidin-5-ylboronicacid (56 mg, 0.34 mmol) according the procedure reported in Scheme 100gave after workup and purification by flash column chromatography[silica gel (12 g), eluting with CMA80 in CHCl₃ 0 to 20%]2-(3-acetyl-6-(2-(dimethylamino)pyrimidin-5-yl)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(204a) (85 mg, 0.15 mmol, 53% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.73 (s, 2H), 8.51 (t, J=5.9 Hz, 1H), 8.29 (s, 1H), 8.19 (d,J=8.3 Hz, 1H), 7.69 (bs, 1H), 7.49 (dd, J=8.3, 1.5 Hz, 1H), 7.39-7.30(m, 1H), 7.24-7.16 (m, 1H), 6.97-6.86 (m, 1H), 5.49 (s, 2H), 4.36 (d,J=5.8 Hz, 2H), 4.01 (s, 2H), 3.19-3.11 (m, 7H), 2.44 (s, 3H), 1.03-0.96(m, 2H), 0.96-0.88 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.72; MS(ES+): 577.5 (M+1); MS (ES−): 611.4 (M+Cl).

Preparation of2-(3-acetyl-6-(pyrimidin-5-yl)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(205a)

Reaction of2-(3-acetyl-6-bromo-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(202e) (150 mg, 0.28 mmol) with pyrimidin-5-ylboronic acid (42 mg, 0.34mmol) according the procedure reported in Scheme 100 gave after workupand purification by flash column chromatography [silica gel (12 g),eluting with CMA80 in CHCl₃ 0 to 20%]2-(3-acetyl-6-(pyrimidin-5-yl)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(205a) (60 mg, 0.11 mmol, 40% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 9.18 (s, 2H), 9.12 (s, 1H), 8.51 (t, J=5.9 Hz, 1H), 8.38 (s,1H), 8.29 (d, J=8.3 Hz, 1H), 7.92 (d, J=1.6 Hz, 1H), 7.67 (dd, J=8.3,1.6 Hz, 1H), 7.34 (td, J=7.7, 7.2, 1.7 Hz, 1H), 7.21-7.12 (m, 1H), 6.88(td, J=7.9, 1.1 Hz, 1H), 5.54 (s, 2H), 4.35 (d, J=5.7 Hz, 2H), 4.01 (s,2H), 3.23-3.11 (m, 1H), 2.46 (s, 3H), 1.05-0.97 (m, 2H), 0.97-0.90 (m,2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.60; MS (ES+): 534.5 (M+1), MS(ES−): 532.4 (M−1), 568.4 (M+Cl).

Preparation of methyl3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylate(206d) Step-1: Preparation of methyl1-(2-(tert-butoxy)-2-oxoethyl)-3-(1-ethoxyvinyl)-1H-indazole-5-carboxylate(206a)

To a solution of methyl1-(2-(tert-butoxy)-2-oxoethyl)-3-iodo-1H-indazole-5-carboxylate (132c)(9.2 g, 22.10 mmol) in toluene (75 mL) under Argon atmosphere was addedtributyl(1-ethoxyvinyl)stannane (9.98 g, 27.6 mmol), Pd(Ph₃P)₄ (2.55 g,2.210 mmol) and heated at 120° C. for 15h. The reaction mixture wascooled to room temperature, diluted with EtOAc (200 mL), filteredthrough a Celite pad. The filtrate was washed with water, brine, driedand concentrated in vacuum. The residue obtained was purified bychromatography [silica (40 g), eluting with EtOAc in hexane 0 to 40%] toafford methyl1-(2-(tert-butoxy)-2-oxoethyl)-3-(1-ethoxyvinyl)-1H-indazole-5-carboxylate(206a) (7.5 g, 19.31 mmol, 87% yield) as a yellow oil; ¹H NMR (300 MHz,DMSO-d₆) δ 8.67 (dd, J=1.6, 0.8 Hz, 1H), 7.97 (dd, J=8.9, 1.6 Hz, 1H),7.73 (dd, J=8.9, 0.8 Hz, 1H), 5.34 (s, 2H), 4.97 (d, J=2.3 Hz, 1H), 4.46(d, J=2.3 Hz, 1H), 4.03 (q, J=6.9 Hz, 2H), 3.88 (s, 3H), 1.45 (m, 3H),1.40 (s, 9H), 0.85 (t, J=7.2 Hz, 3H); MS (ES+): 361.5 (M+1), 383.5(M+Na); MS (ES−): 359.3 (M−1).

Step-2: Preparation of methyl3-acetyl-1-(2-(tert-butoxy)-2-oxoethyl)-1H-indazole-5-carboxylate (206b)

To a solution of methyl1-(2-(tert-butoxy)-2-oxoethyl)-3-(1-ethoxyvinyl)-1H-indazole-5-carboxylate(206a) from step-1 in EtOAc (200 mL) was added HCl (1 N, 120 mL) andsonicated for 10 min. The organic phase was separated, dried,concentrated in vacuum to afford methyl3-acetyl-1-(2-(tert-butoxy)-2-oxoethyl)-1H-indazole-5-carboxylate (206b)(6.2 g, 18.65 mmol, 84% yield over 2 steps) as a white solid, which wasused in the next step without further purification; ¹H NMR (300 MHz,DMSO-d₆) δ 8.84 (dd, J=1.6, 0.8 Hz, 1H), 8.06 (dd, J=8.9, 1.6 Hz, 1H),7.89 (dd, J=8.9, 0.9 Hz, 1H), 5.51 (s, 2H), 3.91 (s, 3H), 2.65 (s, 3H),1.42 (s, 9H); MS (ES⁺), 355.4 (M+Na); 331.4 (M−1).

Step-3: Preparation of2-(3-acetyl-5-(methoxycarbonyl)-1H-indazol-1-yl)acetic acid (206c)

Reaction of methyl3-acetyl-1-(2-(tert-butoxy)-2-oxoethyl)-1H-indazole-5-carboxylate (206b)(6.1 g, 18.35 mmol) with TFA (7.07 mL, 92 mmol) in DCM (50 mL) accordingto the procedure reported in step-2 of Scheme 2 gave after workup2-(3-acetyl-5-(methoxycarbonyl)-1H-indazol-1-yl)acetic acid (206c) (5.8g, 14.86 mmol, 81% yield) TFA salt as an off white solid, which was usedin the next step without further purification; ¹H NMR (300 MHz, DMSO-d₆)δ 13.00 (s, 1H), 8.83 (dd, J=1.7, 0.8 Hz, 1H), 8.08-7.99 (m, 1H), 7.91(dd, J=8.9, 0.8 Hz, 1H), 5.51 (s, 2H), 3.91 (s, 3H), 2.65 (s, 3H); MS(ES⁻): 275.3 (M−1)

Step-4: Preparation of methyl3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylate(206d)

Reaction of 2-(3-acetyl-5-(methoxycarbonyl)-1H-indazol-1-yl)acetic acid(206c) TFA adduct (1.9 g, 4.87 mmol) withN-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide (19c) (1.51 g,5.84 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column [silica (12 g),eluting with DMA80 in DCM 0 to 40%] methyl3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylate(206d) (2.24 g, 4.33 mmol, 89% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.89-8.29 (m, 2H), 8.04 (dd, J=8.9, 1.7 Hz) and 7.97 (dd,J=8.9, 1.7 Hz) (2dd, 1H), 7.77 (dd, J=8.9, 0.8 Hz) and 7.70 (dd, J=8.9,0.8 Hz) (2dd, 1H), 7.56-6.95 (m, 3H), 5.76 and 5.59 (2s, 2H), 4.69-4.23(m, 3H), 4.18 and 3.85 (2s, 2H), 3.913 and 3.908 (2s, 3H), 2.64 (s, 3H),1.26 (d, J=6.7 Hz) and 1.00 (d, J=6.8 Hz) (2d, 6H); ¹⁹F NMR (282 MHz,DMSO) δ −121.21, −121.72; MS (ES+): 517.5 (M+1), 539.5 (M+Na); MS (ES−):515.5 (M−1).

Preparation of methyl3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-6-carboxylate(207g) Step-1: Preparation of methyl 3-iodo-1H-indazole-6-carboxylate(207b)

Compound methyl 3-iodo-1H-indazole-6-carboxylate (207b) was preparedfrom methyl 1H-indazole-6-carboxylate (15 g, 85 mmol) according to theprocedure reported in step-1 of Scheme 132 to furnish product (22 g,72.8 mmol, 86% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ13.82 (s, 1H, D₂O exchangeable), 8.16-8.08 (m, 1H), 7.71 (dd, J=8.6, 1.4Hz, 1H), 7.53 (dd, J=8.6, 0.8 Hz, 1H), 3.88 (s, 3H); MS (ES+); 303.2(M+1); MS (ES−):

301.2 (M−1).

Step-2: Preparation of methyl1-(2-(tert-butoxy)-2-oxoethyl)-3-iodo-1H-indazole-6-carboxylate (207c)

Reaction of methyl 3-iodo-1H-indazole-6-carboxylate (207b) (12 g, 39.7mmol) with tert-butyl 2-bromoacetate (11.62 g, 59.6 mmol) according tothe procedure reported in step-1 of Scheme 56 gave after workup methyl1-(2-tert-butoxy-2-oxoethyl)-3-iodo-1H-indazole-6-carboxylate (207c)(11.7 g, 28.1 mmol, 71% yield) as an off white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.37 (t, J=1.1 Hz, 1H), 7.78 (dd, J=8.5, 1.3 Hz, 1H), 7.56(dd, J=8.5, 0.8 Hz, 1H), 5.44 (s, 2H), 3.91 (s, 3H), 1.40 (s, 9H); MS(ES+): 439.4 (M+Na).

Step-3: Preparation of methyl1-(2-(tert-butoxy)-2-oxoethyl)-3-cyano-1H-indazole-6-carboxylate (207d)

A mixture of methyl1-(2-tert-butoxy-2-oxoethyl)-3-iodo-1H-indazole-6-carboxylate (207c)(10.7 g, 25.7 mmol), zinc (0.336 g, 5.14 mmol), zinc cyanide (3.62 g,30.8 mmol), Pd₂(dba)₃, (1.883 g, 2.06 mmol), Xantphos (1.488 g, 2.57mmol), TMEDA (0.776 mL, 5.14 mmol) in DMF (75 mL) was purged with Argonfor 5 mins and heated at 100° C. for 6 h. The reaction mixture wascooled to room temperature, diluted with EtOAc (250 mL), and filteredthrough Celite, rinsing with EtOAc (2×100 mL). The filtrate wasconcentrated to dryness and the residue was triturated with MeOH (10mL). The solid obtained was collected by filtration washed with MeOH(2×3 mL), dried to give methyl1-(2-tert-butoxy-2-oxoethyl)-3-cyano-1H-indazole-6-carboxylate (207d)(5.28 g, 16.74 mmol, 65.1% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.61 (t, J=1.1 Hz, 1H), 8.05 (dd, J=8.6, 0.8 Hz, 1H), 7.95(dd, J=8.6, 1.3 Hz, 1H), 5.65 (s, 2H), 3.93 (s, 3H), 1.41 (s, 9H); MS(ES+): 338.4 (M+Na); MS (ES−): 314.3 (M−1).

Step-4: Preparation of methyl1-(2-(tert-butoxy)-2-oxoethyl)-3-carbamoyl-1H-indazole-6-carboxylate(207e)

Reaction of methyl1-(2-(tert-butoxy)-2-oxoethyl)-3-cyano-1H-indazole-6-carboxylate (207d)(5.18 g, 16.42 mmol) in ethanol (50 mL) using conc. NH₄OH (30 mL) andH₂O₂ (aq. 35%, 10.16 mL, 99 mmol) according to the procedure reported inScheme 65 gave after workup methyl1-(2-tert-butoxy-2-oxoethyl)-3-carbamoyl-1H-indazole-6-carboxylate(207e) (3.4 g, 10.18 mmol, 62% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.43 (t, J=1.1 Hz, 1H), 8.30 (dd, J=8.6, 0.8 Hz, 1H),7.90-7.81 (m, 2H), 7.54 (s, 1H), 5.49 (s, 2H), 3.92 (s, 3H), 1.41 (s,9H); MS (ES+): 333.4 (M+1)

Step-5: Preparation of2-(3-carbamoyl-6-(methoxycarbonyl)-1H-indazol-1-yl)acetic acid (207f)

Reaction of methyl1-(2-(tert-butoxy)-2-oxoethyl)-3-carbamoyl-1H-indazole-5-carboxylate(207e) (3.3 g, 9.9 mmol) with TFA (3.81 mL, 49.5 mmol) in DCM (50 mL)according to the procedure reported in step-2 of Scheme 2 gave afterworkup 2-(3-carbamoyl-6-(methoxycarbonyl)-1H-indazol-1-yl)acetic acid(207f) TFA salt (2.8 g, 7.16 mmol, 72% yield) as a white solid, whichwas used in the next step without further purification; ¹H NMR (300 MHz,DMSO-d₆) δ 13.37 (s, 1H), 8.47-8.41 (m, 1H), 8.35-8.24 (m, 1H),7.90-7.80 (m, 2H), 7.54 (s, 1H), 5.50 (s, 2H), 3.91 (s, 3H); MS (ES+):278.3 (M+1); MS (ES−): 276.2 (M−1).

Step-6: Preparation of methyl3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-6-carboxylate(207g)

Reaction of 2-(3-carbamoyl-6-(methoxycarbonyl)-1H-indazol-1-yl)aceticacid (207f) TFA adduct (1.82 g, 4.65 mmol) withN-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide (10b) (1.43 g,5.58 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column [silica (40 g),eluting with DMA80 in DCM 0 to 40%] methyl3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-6-carboxylate(207g) (1.6 g, 3.10 mmol, 67% yield) as a yellow solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.52 (t, J=5.9 Hz, 1H), 8.38 (t, J=1.1 Hz, 1H), 8.29 (dd,J=8.5, 0.8 Hz, 1H), 7.87 (s, 1H), 7.83 (dd, J=8.6, 1.3 Hz, 1H), 7.50 (s,1H), 7.44 (ddd, J=8.8, 7.3, 1.7 Hz, 1H), 7.21 (td, J=7.3, 6.8, 1.7 Hz,1H), 7.06 (td, J=7.9, 1.1 Hz, 1H), 5.80 (s, 2H), 4.33 (d, J=5.7 Hz, 2H),3.99 (s, 2H), 3.88 (s, 3H), 3.17-3.04 (m, 1H), 1.07-0.99 (m, 2H),0.97-0.88 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.65; MS (ES+): 538.5(M+Na); (ES−): 514.4 (M−1).

Preparation of3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-6-carboxylicacid (208a)

Reaction of methyl3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-6-carboxylate(207g) (1.6 g, 3.10 mmol) in MeOH (25 mL) and water (25 mL) with lithiumhydroxide hydrate (0.78 g, 18.61 mmol) according to the procedurereported in step-2 of Scheme 129 gave after workup3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-6-carboxylicacid (208a) (1.3 g, 2.59 mmol, 84% yield) as an off white solid, whichwas used in the next step without further purification; ¹H NMR (300 MHz,DMSO-d₆) δ 13.18 (s, 1H), 8.52 (t, J=5.8 Hz, 1H), 8.36 (s, 1H), 8.26 (d,J=8.5 Hz, 1H), 7.95-7.76 (m, 2H), 7.58-7.39 (m, 2H), 7.34-7.18 (m, 1H),7.09 (t, J=7.9 Hz, 1H), 5.79 (s, 2H), 4.33 (d, J=5.7 Hz, 2H), 3.99 (s,2H), 3.14-2.98 (m, 1H), 1.09-0.97 (m, 2H), 0.97-0.83 (m, 2H); ¹⁹F NMR(282 MHz, DMSO-d₆) δ −121.60; MS (ES+): 502.4 (M+1); MS (ES−) 500.4(M−1).

Preparation ofN-(3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indol-5-yl)-3,3-difluoropiperidine-1-carboxamide(209b) Step-1: Preparation of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indole-5-carbonylazide (209a)

Compound3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indole-5-carbonylazide (209a) was prepared from3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indole-5-carboxylicacid (165b) (1.8 g, 3.60 mmol) according to the procedure reported instep-3 of Scheme 129 to afford product; MS (ES−): 523.4 (M−1).

Step-2: Preparation ofN-(3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indol-5-yl)-3,3-difluoropiperidine-1-carboxamide(209b)

Compound (209b) was prepared from3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indole-5-carbonylazide (209a) (200 mg, 0.38 mmol) and 3,3-difluoropiperidinehydrochloride (120 mg, 0.76 mmol) using TEA (0.21 mL, 1.51 mmol) as baseaccording to the procedure reported in step-4 of Scheme 129 to affordafter workup and purification by column chromatography [silica gel (12g), eluting with DMA80 in DCM 0 to 40%] (45 mg, 0.073 mmol, 19%) as awhite solid; ¹H NMR (300 MHz, DMSO-d₆) δ 8.65 (s, 1H), 8.47 (t, J=5.8Hz, 1H), 8.21 (s, 1H), 8.19 (s, 1H), 7.45 (t, J=7.6 Hz, 1H), 7.41-7.28(m, 2H), 7.24 (t, J=7.1 Hz, 1H), 7.12 (t, J=7.9 Hz, 1H), 5.39 (s, 2H),4.35 (d, J=5.7 Hz, 2H), 4.00 (s, 2H), 3.81 (t, J=12.1 Hz, 2H), 3.52 (t,J=5.3 Hz, 2H), 3.17-2.97 (m, 1H), 2.41 (s, 3H), 2.16-1.94 (m, 2H),1.79-1.59 (m, 2H), 1.04-0.88 (m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−101.12, −121.63; MS (ES+): 618.6 (M+1); MS (ES−): 616.5 (M−1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((cis)-3-(hydroxymethyl)cyclobutyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(210b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-(((cis)-3-(hydroxymethyl)cyclobutyl)amino)acetamide(210a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (300 mg,1.27 mmol) with ((cis)-3-aminocyclobutyl)methanol hydrochloride (262 mg,1.91 mmol) according to the procedure reported in step-2 of Scheme 35gave after workupN-(3-chloro-2-fluorobenzyl)-2-(((cis)-3-(hydroxymethyl)cyclobutyl)amino)acetamide(210a) a an oil which was used in the next step without furtherpurification; MS (ES+): 301.4 (M+1); MS (ES−): 299.4 (M−1).

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((cis)-3-(hydroxymethyl)cyclobutyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(210b)

Reaction ofN-(3-chloro-2-fluorobenzyl)-2-(((cis)-3-(hydroxymethyl)cyclobutyl)amino)acetamide(210a) (169 mg, 0.56 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (123 mg, 0.56 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with MeOH in DCM 0 to 30%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((cis)-3-(hydroxymethyl)cyclobutyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(210b) (53 mg, 0.11 mmol, 19% yield) as a white solid as a mixture oftwo rotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 8.89 (t, J=5.8 Hz) & 8.42 (t,J=5.9 Hz) (2t, 1H), 8.23-8.13 (m, 1H), 7.70 (s, 1H), 7.62-7.00 (m, 7H),5.56 & 5.40 (2s, 2H), 4.59 & 4.52 (t, J=5.2 Hz) (2t, 1H, D₂Oexchangeable), 4.55-4.37 (m, 1H), 4.47 (d, J=6.2 Hz) & 4.34 (d, J=5.9 Hz(2d, 2H), 4.28 & 4.01 (2s, 2H), 3.43-3.28 (m, 2H), 2.34-1.66 (m, 5H);¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.25, −121.66; MS (ES+): 502.5 (M+1),524.5, 526.5 (M+Na); MS (ES−): 500.4 (M−1), 536.4 (M+Cl).

Preparation of5-(3-benzylureido)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(211a)

Reaction of3-carbamoyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (145a) (150 mg, 0.284 mmol) in toluene (15 mL) withphenylmethanamine (60.8 mg, 0.567 mmol) using TEA (0.16 mL, 1.13 mmol)as base according to the procedure reported in step-4 of Scheme 129 gaveafter workup and purification by column chromatography [silica gel (12g), eluting with DMA80 in DCM 0 to 40%]5-(3-benzylureido)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(211a) (11 mg, 0.018 mmol, 6% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) (a mixture of two rotamers) δ 8.81 (t, J=5.7 Hz) and 8.36 (t,J=5.9 Hz) (2t, 1H), 8.74-8.64 (m, 1H), 8.24 and 8.20 (2s, 1H), 7.63-7.54(m, 1H), 7.52-6.99 (m, 11H), 6.58 (t, J=5.7 Hz, 1H), 5.52 and 5.39 (2s,2H), 4.61-4.23 (m, 5H), 4.17 and 3.83 (2s, 2H), 1.21 (d, J=6.5 Hz) and0.98 (d, J=6.8 Hz) (2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.23,−121-76; MS (ES+): 608.6 (M+1); MS (ES−): 606.6 (M−1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(pyrimidin-5-yl)-1H-indazole-3-carboxamide(212a)

Reaction of5-bromo-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(140a) (125 mg, 0.23 mmol) with pyrimidin-5-ylboronic acid (32 mg, 0.256mmol) according the procedure reported in Scheme 100 gave after workupand purification by flash column chromatography [silica gel (12 g),eluting with DMA80-DCM 0 to 30%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(pyrimidin-5-yl)-1H-indazole-3-carboxamide(212a) (69 mg, 0.13 mmol, 55% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 9.21 (s, 1H), 9.17 (s, 2H), 8.56-8.44 (m, 2H), 7.89-7.78 (m,3H), 7.54-7.39 (m, 2H), 7.27-7.19 (m, 1H), 7.17-7.07 (m, 1H), 5.73 (s,2H), 4.34 (d, J=5.7 Hz, 2H), 4.00 (s, 2H), 3.15-3.02 (m, 1H), 1.08-0.96(m, 2H), 0.99-0.86 (m, 2H); 19F NMR (282 MHz, DMSO-d₆) δ −121.57; MS(ES+): 536.6 (M+1), 558.5 (M+Na); MS (ES−): 534.5 (M−1), 570.5 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(4-methylpiperazine-1-carboxamido)-1H-indazole-3-carboxamide(213a)

Reaction of3-carbamoyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (145a) (150 mg, 0.284 mmol) in toluene (15 mL) with1-methylpiperazine (56.8 mg, 0.567 mmol) using TEA (0.16 mL, 1.13 mmol)as base according to the procedure reported in step-4 of Scheme 129 gaveafter workup and purification by column chromatography [silica gel (12g), eluting with DMA80 in DCM 0 to 40%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(4-methylpiperazine-1-carboxamido)-1H-indazole-3-carboxamide(213a) (31 mg, 0.052 mmol, 18% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) (mixture of two rotamers) δ 8.82 (t, J=5.7 Hz) and 8.36 (t,J=5.8 Hz) (2t, 1H), 8.65 (s, 1H), 8.19-8.15 (m, 1H), 7.64-7.01 (m, 7H),5.53 and 5.39 (2s, 2H), 4.60-4.25 (m, 3H), 4.17 and 3.83 (2s, 2H),3.50-3.43 (m, 4H), 2.39-2.31 (m, 4H), 2.23 (s, 3H), 1.21 (d, J=6.6 Hz)and 0.98 (d, J=6.8 Hz) (2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.22,−121.79; MS (ES+): 601.5 (M+1); MS (ES): 599.5 (M−1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-((4-methylpyrimidin-2-yl)methoxy)-1H-indazole-3-carboxamide(214e) Step-1: Preparation of tert-butyl2-(3-carbamoyl-5-hydroxy-1H-indazol-1-yl)acetate (214b)

A mixture of tert-butyl 2-(3-cyano-5-hydroxy-1H-indazol-1-yl)acetate(214a) (Prepared according to the procedure reported by Altmann, Eva etal; in PCT Int. Appl., WO 2014/002053, 360 mg, 1.32 mmol), palladium(II)acetate (30 mg, 0.13 mmol), triphenylphosphine (69 mg, 0.26 mmol)acetaldehyde oxime (0.16 mL, 2.63 mmol) in ethanol (8 mL) and water (2mL) was heated to 90° C. for 2 h. The reaction mixture was cooled toroom temperature, diluted with EtOAc (50 mL), filtered through a Celitepad and evaporated to dryness. The residue obtained was purified byflash column chromatography [Silica gel, (12 g) eluting with EtOAc inhexanes 0-100%] to afford tert-butyl2-(3-carbamoyl-5-hydroxy-1H-indazol-1-yl)acetate (214b) (351 mg, 1.21mmol, 91% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 9.41 (s,1H), 7.67-7.47 (m, 3H), 7.28 (s, 1H), 6.97 (dd, J=8.9, 2.4 Hz, 1H), 5.26(s, 2H), 1.41 (s, 9H); MS (ES+): 292.1 (M+1), MS (ES−): 290.3 (M−1).

Step-2: Preparation of tert-butyl2-(3-carbamoyl-5-((4-methylpyrimidin-2-yl)methoxy)-1H-indazol-1-yl)acetate(214c)

To a solution of tert-butyl2-(3-carbamoyl-5-hydroxy-1H-indazol-1-yl)acetate (214b) (201 mg, 0.69mmol) in DMF (5 mL) was added cesium carbonate (0.28 g, 0.863 mmol) and2-(chloromethyl)-4-methylpyrimidine (108 mg, 0.759 mmol). The reactionmixture was stirred at room temperature for 13 h and quenched with coldwater (50 mL). The solid obtained was collected by filtration, washedwith water (2×25 mL), dried under reduced pressure over P₂O₅ to furnishtert-butyl2-(3-carbamoyl-5-((4-methylpyrimidin-2-yl)methoxy)-1H-indazol-1-yl)acetate(214c) (152 mg, 0.38 mmol, 55% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.66 (d, J=5.1 Hz, 1H), 7.67-7.60 (m, 2H), 7.59 (d, J=2.4 Hz,1H), 7.38-7.32 (m, 2H), 7.20 (dd, J=9.1, 2.4 Hz, 1H), 5.30 (s, 2H), 5.25(s, 2H), 2.49 (s, 3H), 1.41 (s, 9H); MS (ES+): 398.5 (M+1), 795.9(2M+1); MS (ES−): 396.4 (M−1).

Step-3: Preparation of2-(3-carbamoyl-5-((4-methylpyrimidin-2-yl)methoxy)-1H-indazol-1-yl)aceticacid (214d)

Reaction of tert-butyl2-(3-carbamoyl-5-((4-methylpyrimidin-2-yl)methoxy)-1H-indazol-1-yl)acetate(214c) (138 mg, 0.35 mmol) with TFA (0.54 mL, 6.94 mmol) in DCM (10 mL)according to the procedure reported in step-2 of Scheme 2 gave afterworkup and trituration with hexanes,2-(3-carbamoyl-5-((4-methylpyrimidin-2-yl)methoxy)-1H-indazol-1-yl)aceticacid (214d) (148 mg, 0.33 mmol, 94% yield) TFA salt as an off whitesolid; ¹H NMR (300 MHz, DMSO-d₆) δ 13.4 (bs, 1H), 8.67 (d, J=5.1 Hz,1H), 7.68-7.62 (m, 2H), 7.58 (d, J=2.4 Hz, 1H), 7.39-7.29 (m, 2H), 7.19(dd, J=9.1, 2.4 Hz, 1H), 5.31 (s, 2H), 5.26 (s, 2H), 2.49 (s, 3H); MS(ES+): 342.4 (M+1).

Step-4: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-((4-methylpyrimidin-2-yl)methoxy)-1H-indazole-3-carboxamide(214e)

Reaction of2-(3-carbamoyl-5-((4-methylpyrimidin-2-yl)methoxy)-1H-indazol-1-yl)aceticacid (214d) TFA (103 mg, 0.23 mmol withN-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide (19c) (70 mg,0.27 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column [silica (12 g),eluting with DMA80 in DCM, 0 to 100%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-((4-methylpyrimidin-2-yl)methoxy)-1H-indazole-3-carboxamide(214e) (94 mg, 0.16 mmol, 71% yield) as an off-white solid as a mixtureof two rotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 8.82 (t, J=5.7 Hz) & 8.36(t, J=6.1 Hz) (2t, 1H), 8.67 (d, J=5.1 Hz, 1H), 7.61-6.98 (m, 9H), 5.54& 5.40 (2s, 2H), 5.26 & 5.25 (2s, 2H), 4.60-4.49 & 4.28-4.22 (2m, 1H),4.46 (d, J=5.5 Hz) & 4.32 (d, J=5.8 Hz) (2d, 2H), 4.16 & 3.83 (2s, 2H),2.49 (s, 3H), 1.25 (d) & 0.98 (d, J=6.8 Hz) (2d, 6H); ¹⁹F NMR (282 MHz,DMSO-d₆) δ −121.22, −121.76; MS (ES+): 582.6 & 584.6 (M+1), 604.6, 606.6(M+Na); MS (ES−): 580.5 (M−1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(3-(pyrimidin-5-yl)ureido)-1H-indazole-3-carboxamide(215a)

Reaction of3-carbamoyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (145a) (150 mg, 0.284 mmol) in toluene (15 mL) withpyrimidin-5-amine (54 mg, 0.57 mmol) using TEA (0.16 mL, 1.13 mmol) asbase according to the procedure reported in step-4 of Scheme 129 gaveafter workup and purification by column chromatography [silica gel (12g), eluting with DMA80 in DCM 0 to 40%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(3-(pyrimidin-5-yl)ureido)-1H-indazole-3-carboxamide(215a) (14 mg, 0.023 mmol, 8% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 9.36-9.09 (m, 2H), 8.044 and 8.935 (2s, 2H), 8.88-8.29 (m,3H), 7.71-7.59 (m, 1H), 7.57-6.99 (m, 6H), 5.56 and 5.42 (2s, 2H),4.64-4.25 (m, 3H), 4.18 and 3.84 (2s, 2H), 1.22 (d, J=6.3 Hz) and 0.99(d, J=6.7 Hz) (2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.22, −121-75;MS (ES+) 596.6 (M+1); (ES−) 594.5 (M−1).

Preparation of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (216a)

Reaction of methyl3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylate(206d) (2.24 g, 4.33 mmol) in MeOH (25 mL) and water (25 mL) withlithium hydroxide hydrate (1.091 g, 26.0 mmol) according to theprocedure reported in step-2 of Scheme 129 gave after workup3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (216a) (2.1 g, 4.18 mmol, 96% yield) as an off white solid, whichwas used in the next step without further purification; ¹H NMR (300 MHz,DMSO-d₆) (a mixture of two rotamers) δ 13.07 (s, 1H), 9.21 (t, J=5.8 Hz)and 8.62 (t, J=6.0 Hz) (2t, 1H), 8.86-8.77 (m, 1H)), 8.05-7.64 (m, 2H),7.55-6.88 (m, 3H), 5.81 and 5.60 (2s, 2H), 4.64-4.20 (m, 3H), 4.26 and3.84 (2s, 2H), 2.64 and 2.29 (2s, 3H), 1.26 (d, J=6.4 Hz) and 1.00 (d,J=6.8 Hz) (2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.29, −121.81; MS(ES+): 502.4 (M+1); (ES−): 500.4 (M−1).

Preparation ofN-(3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazol-5-yl)-3,3-difluoropiperidine-1-carboxamide(217b) Step-1: Preparation of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (217a)

Compound3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (217a) was prepared from3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (216a) (950 mg, 1.889 mmol) according to the procedure reported instep-3 of Scheme 129 to afford product (1.4 g, 2.65 mmol, 140% yield),which was used in the next step without further purification. MS (ES+):528.5 (M+1).

Step-2: Preparation ofN-(3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazol-5-yl)-3,3-difluoropiperidine-1-carboxamide(217b)

Compound (217b) was prepared from3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (217a) (220 mg, 0.42 mmol) and 3,3-difluoropiperidinehydrochloride (131 mg, 0.83 mmol) using TEA (0.23 mL, 1.67 mmol) as baseaccording to the procedure reported in step-4 of Scheme 129 to affordafter workup and purification by column chromatography [silica gel (12g), eluting with DMA80 in DCM 0 to 40%] (32 mg, 0.052 mmol, 12.36%yield) product as a white solid; ¹H NMR (300 MHz, DMSO-d₆) (mixture oftwo rotamers) δ 8.93-8.31 (m, 2H), 8.24 (bs, 1H), 7.65-7.00 (m, 5H),5.64 and 5.48 (2s, 2H), 4.66-4.23 (m, 3H), 4.17 and 3.78 (2s, 2H),3.88-3.80 (m, 2H), 3.61-3.47 (m, 2H), 2.59 (s, 3H), 2.19-1.95 (m, 2H),1.84-1.60 (m, 2H), 1.24 (d, J=6.4 Hz) and 1.00 (d, J=6.8 Hz) (2d, 6H);¹⁹F NMR (282 MHz, DMSO-d₆) δ −101.15, −121.22, −121.78; MS (ES+): 621.7(M+1); (ES−): 619.6 (M−1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(2-(dimethylamino)pyrimidin-5-yl)-1H-indazole-3-carboxamide(218a)

Reaction of5-bromo-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(140a) (125 mg, 0.23 mmol) with 2-(dimethylamino)pyrimidin-5-ylboronicacid (43 mg, 0.26 mmol) according the procedure reported in Scheme 100gave after workup and purification by flash column chromatography[silica gel (12 g), eluting with DMA80-DCM 0 to 30%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(2-(dimethylamino)pyrimidin-5-yl)-1H-indazole-3-carboxamide(218a) (42 mg, 0.073 mmol, 31% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.69 (s, 2H), 8.50 (t, J=5.9 Hz, 1H), 8.28 (dd, J=1.7, 0.9Hz, 1H), 7.80-7.62 (m, 3H), 7.51-7.39 (m, 2H), 7.28-7.19 (m, 1H), 7.12(td, J=7.9, 1.0 Hz, 1H), 5.69 (s, 2H), 4.33 (d, J=5.7 Hz, 2H), 3.99 (s,2H), 3.18 (s, 6H), 3.13-3.02 (m, 1H), 1.05-0.96 (m, 2H), 0.97-0.86 (m,2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.57; MS (ES+): 579.6 (M+1), 601.6(M+Na); MS (ES−): 577.5 (M−1), 613.6 (M+Cl).

Preparation ofN-(3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indol-6-yl)-3,3-difluoropiperidine-1-carboxamide(219b) Step-1: Preparation of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indole-6-carbonylazide (219a)

Compound (219a) was prepared from3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indole-6-carboxylicacid (201a) (1.98 g, 3.96 mmol) according to the procedure reported instep-3 of Scheme 129 to afford product (219a) (2.2 g, 4.19 mmol, 106%yield) which was used in the next step without further purification; MS(ES−): 523.5 (M−1).

Step-2: Preparation ofN-(3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indol-6-yl)-3,3-difluoropiperidine-1-carboxamide(219b)

Compound (219b) was prepared from3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indole-6-carbonylazide (219a) (200 mg, 0.38 mmol) and 3,3-difluoropiperidinehydrochloride (120 mg, 0.76 mmol) using TEA (0.21 mL, 1.51 mmol) as baseaccording to the procedure reported in step-4 of Scheme 129 to affordafter workup and purification by column chromatography [silica gel (12g), eluting with DMA80 in DCM 0 to 40%] (17 mg, 0.028 mmol, 7% yield) asa white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 8.66 (s, 1H), 8.47 (t, J=5.8Hz, 1H), 8.19 (s, 1H), 8.01 (d, J=8.6 Hz, 1H), 7.58 (d, J=1.8 Hz, 1H),7.50-7.41 (m, 1H), 7.28-7.20 (m, 2H), 7.17-7.09 (m, 1H), 5.35 (s, 2H),4.34 (d, J=5.7 Hz, 2H), 4.00 (s, 2H), 3.79 (t, J=12.1 Hz, 2H), 3.56-3.46(m, 2H), 3.13-3.01 (m, 1H), 2.40 (s, 3H), 2.16-1.95 (m, 2H), 1.78-1.59(m, 2H), 1.02-0.98 (m, 2H), 0.97-0.90 (m, 2H); ¹⁹F NMR (282 MHz,DMSO-d₆) δ −101.11, −121.65; MS (ES+): 618.6 (M+1); MS (ES−): 616.6(M−1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(3-(pyridin-3-yl)ureido)-1H-indazole-3-carboxamide(220a)

Reaction of3-carbamoyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (145a) (150 mg, 0.28 mmol) in toluene (15 mL) with pyridin-3-amine(53 mg, 0.57 mmol) using TEA (0.16 mL, 1.13 mmol) as base according tothe procedure reported in step-4 of Scheme 129 gave after workup andpurification by column chromatography [silica gel (12 g), eluting withDMA80 in DCM 0 to 40%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(3-(pyridin-3-yl)ureido)-1H-indazole-3-carboxamide(220a) (22 mg, 0.037 mmol, 13.04% yield) as a white solid; ¹H NMR (300MHz, DMSO-d₆) (mixture of two rotamers) δ 8.98 and 8.96 (2s, 1H),8.90-8.77 and 8.41-8.30 (2m, 3H), 8.66-8.56 (m, 1H), 8.22-8.13 (m, 1H),8.02-7.91 (m, 1H), 7.67-6.99 (m, 8H), 5.55 and 5.42 (2s, 2H), 4.64-4.23(m, 3H), 4.18 and 3.83 (2s, 2H), 1.22 (d, J=6.3 Hz) and 0.99 (d, J=6.7Hz) (2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.21, −121.74; MS (ES+):595.6 (M+1); (ES−): 593.5 (M−1)

Preparation ofN-(3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazol-5-yl)morpholine-4-carboxamide(221a)

Reaction of3-carbamoyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (145a) (150 mg, 0.28 mmol) in toluene (15 mL) with morpholine(49.4 mg, 0.57 mmol) using TEA (0.16 mL, 1.13 mmol) as base according tothe procedure reported in step-4 of Scheme 129 gave after workup andpurification by column chromatography [silica gel (12 g), eluting withDMA80 in DCM 0 to 40%]N-(3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazol-5-yl)morpholine-4-carboxamide (221a) (33 mg, 0.056mmol, 20% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 8.81 and8.36 (2t, J=5.7 Hz, 1H), 8.67 (s, 1H), 8.22-8.15 (m, 1H), 7.65-7.00 (m,7H), 5.53 and 5.40 (2s, 2H), 4.61-4.23 (m, 3H), 4.17 and 3.83 (2s, 2H),3.66-3.56 (m, 4H), 3.47-3.39 (m, 4H), 1.21 (d, J=6.6 Hz) and 0.98 (d,J=6.8 Hz) (2d, 6H); ¹⁹F NMR (282 MHz, DMSO) δ −121.22, −121.78; MS(ES+): 588.6 (M+1); MS (ES−): 586.5 (M−1).

Preparation of(R)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(222b) Step-1: Preparation of(R)—N-(3-chloro-2-fluorobenzyl)-2-((1-hydroxypropan-2-yl)amino)acetamide(222a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (500 mg,2.12 mmol) with (R)-2-aminopropan-1-ol (318 mg, 4.24 mmol) according tothe procedure reported in step-2 of Scheme 35 gave after workup(R)—N-(3-chloro-2-fluorobenzyl)-2-(1-hydroxypropan-2-ylamino)acetamide(222a) (582 mg, 2.12 mmol, 100%) which was used as such in the nextstep; MS (ES+): 275.3 (M+1); MS (ES−): 273.3 (M−1).

Step-2: Preparation of(R)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(222b)

Reaction of (R)—N-(3-chloro-2-fluorobenzyl)-2-((l-hydroxypropan-2-yl)-amino)acetamide (222a) (200 mg, 0.73 mmol) with2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e) (251 mg, 0.91 mmol)according to the procedure reported in step-3 of Scheme 2 gave afterworkup and purification by flash column chromatography [silica (12 g),eluting with CMA80 in CHCl₃ 0 to 60%](R)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(222b) (39 mg, 0.082 mmol, 9% yield) as an off-white solid as a mixtureof two rotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 8.88 (t, J=5.7 Hz) & 8.61(t, J=5.9 Hz) (2t, 1H, D₂O exchangeable), 8.24-8.13 (m, 1H), 7.71 (s,1H), 7.60-6.94 (m, 7H), 5.63 (d, J=3.6 Hz) &5.42 (d, J=2.9 Hz) (2d, 2H),5.51 (t, J=6.0 Hz) & 4.81 (t, J=5.7 Hz) (2t, 1H, D₂O exchangeable),4.59-3.74 (m, 5H), 3.55-3.24 (m, 2H), 1.15 (d, J=6.6 Hz) & 0.96 (d,J=6.9 Hz) (2d, 3H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.26, −121.65; MS(ES+): 498.5 (M+Na); MS (ES−): 474.4 (M−1), 510.4 (M+Cl).

Preparation ofN-(3-acetyl-1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazol-5-yl)-3,3-difluoropiperidine-1-carboxamide(223c) Step-1: Preparation of methyl3-acetyl-1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylate(223a)

Reaction of 2-(3-acetyl-5-(methoxycarbonyl)-1H-indazol-1-yl)acetic acid(206c) TFA adduct (237 g, 0.86 mmol) withN-(2′-chloro-2-fluorobiphenyl-3-yl)-2-(isopropylamino)acetamide (115c)(250 mg, 0.78 mmol) according to the procedure reported in step-3 ofscheme-2 gave after workup and purification by flash column [silica(24g), eluting with DMA80 in DCM 0 to 20%] methyl3-acetyl-1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylate(223a) (280 mg, 0.48 mmol, 62% yield) as a off-white solid; ¹H NMR (300MHz, DMSO-d₆) (mixture of two rotamers) δ 10.27 and 9.74 (2s, 1H), 8.85and 8.83 (dd, J=1.6, 0.8 Hz, 1H), 8.18-6.97 (m, 9H), 5.83 and 5.64 (2s,2H), 4.69-4.57 and 4.38-4.26 (2m, 1H), 4.47 and 4.09 (2s, 2H), 3.918 and3.91 (s, 3H), 2.657 and 2.65 (2s, 3H), 1.29 and 1.07 (2d, J=6.8 Hz, 6H);MS (ES+): 579.6 (M+1), 601.6 (M+Na); MS (ES−): 577.5 (M−1), 613.5(M+Cl).

Step-2: Preparation3-acetyl-1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (223b)

Reaction of methyl3-acetyl-1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylate(223a) (280 mg, 0.48 mmol) in THF (25 mL) with a solution of lithiumhydroxide hydrate (23 mg, 0.97 mmol) in water (1 mL) according to theprocedure reported in step-2 of scheme-29 gave after workup3-acetyl-1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (223b) (250 mg, 0.44 mmol, 92% yield) as a white solid; ¹H NMR (300MHz, DMSO-d₆) (mixture of two rotamers) δ 13.01 (s, 1H), 10.27 and 9.74(2s, 1H), 8.83 and 8.82 (2s, 1H), 8.19-6.97 (m, 9H), 5.81 and 5.63 (2s,2H), 4.70-4.57 and 4.38-4.27 (2m, 1H), 4.47 and 4.09 (s, 2H), 2.65 and2.64 (2s, 3H), 1.29 and 1.07 (2d, J=6.7 Hz, 6H); 19F NMR (282 MHz,DMSO-d₆) δ −126.85, −126.96; MS (ES−): 563.6 & 565.4 (M−1).

Step-3: Preparation ofN-(3-acetyl-1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazol-5-yl)-3,3-difluoropiperidine-1-carboxamide(223c)

To a solution of3-acetyl-1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (223b) (150 mg, 0.27 mmol) in toluene (4 mL) was addedtriethylamine (0.19 mL, 1.33 mmol), diphenyl phosphorazidate (110 mg,0.4 mmol) and stirred at RT for 2h. Dioxane (2 ml) was added to thereaction mixture and heated at 90° C. for 2h. The reaction mixture wascooled to RT, added 3,3-difluoropiperidine hydrochloride (84 mg, 0.53mmol) and continued stirring at 90° C. for 20h. The reaction mixture wascooled to RT, partitioned between 0.5 M aq. HCl (40 ml) and EtOAc (50ml). The aqueous layer was separated and extracted with EtOAc (40 ml).The organic layers were combined washed with saturated aqueous NaHCO₃solution (40 ml), brine, dried, filtered and concentrated in vacuum. Theresidue obtained was purified by flash column chromatography [silica gel(12 g), eluting with MeOH:EtOAc (9:1) in hexanes 0 to 70%] to affordN-(3-acetyl-1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazol-5-yl)-3,3-difluoropiperidine-1-carboxamide(223c) (32 mg, 0.047 mmol, 18% yield) as white solid; ¹H NMR (300 MHz,DMSO-d₆) (mixture of two rotamers) δ 10.26 and 9.75 (2s, 1H), 8.84 and8.82 (2s, 1H), 8.24 and 8.23 (2s, 1H), 8.11 and 7.95 (2t, J=7.8 Hz, 1H),7.67-7.01 (m, 8H), 5.69 and 5.53 (2s, 2H), 4.72-4.56 and 4.38-4.27 (2m,1H), 4.46 and 4.09 (2s, 2H), 3.82 (t, J=12.0 Hz, 2H), 3.58-3.48 (m, 2H),2.595 and 2.588 (2s, 3H), 2.17-1.95 (m, 2H), 1.78-1.64 (m, 2H), 1.27 and1.07 (2d, J=6.8 Hz, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) (mixture of tworotamers) δ −101.15, −126.86 and −126.99; MS (ES+): 683.7 (M+1), 705.7(M+Na), MS (ES−): 717.6 (M+Cl).

Preparation of3-acetyl-N-benzyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxamide(224a)

Reaction of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (216a) (50 mg, 0.1 mmol) with phenylmethanamine (0.017 mL, 0.15mmol) according to the procedure reported in step-3 of Scheme 2 gaveafter workup and purification by flash column [silica (8 g), elutingDCM/MeOH (1:0 to 19:1)]3-acetyl-N-benzyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxamide(224a) (35 mg, 60%) as a white solid as mixture of two rotamers; ¹H NMR(300 MHz, DMSO-d₆) δ 9.25 (t, J=5.9 Hz, 1H), 8.85 (t, J=5.6 Hz) and 8.36(t, J=5.9 Hz) (2t, 1H), 8.79-8.75 (m, 1H), 8.00 (dd, J=8.9, 1.6 Hz,) and7.95 (dd, J=8.9, 1.6 Hz) (2dd, 1H), 7.72 (d) and 7.66 (d, J=8.9 Hz) (2d,1H), 7.58-6.86 (m, 8H), 5.74 and 5.57 (2s, 2H), 4.64-4.22 (m, 5H), 4.19and 3.85 (2s, 2H), 2.69 and 2.64 (s, 3H), 1.26 (d, J=6.5 Hz) and 1.00(d, J=6.7 Hz) (2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.21, −121.74;MS (ES+): 614.7 (M+Na); MS (ES−): 590.6 (M−1), 626.5 (M+Cl).

Preparation of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-N-(1-phenylethyl)-1H-indazole-5-carboxamide(225a)

Reaction of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (216a) (50 mg, 0.1 mmol) with 1-phenylethanamine (0.02 mL, 0.15mmol) according to the procedure reported in step-3 of Scheme 2 gaveafter workup and purification by flash column [silica (8 g), elutingEtOAc/MeOH (1:0 to 19:1)]3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-N-(1-phenylethyl)-1H-indazole-5-carboxamide(225a) (37 mg, 61%) as a white solid as mixture of two rotamers; ¹H NMR(300 MHz, DMSO-d₆) δ 9.08-9.00 (m, 1H), 8.85 (t, J=5.8 Hz) and 8.36 (t,J=5.9 Hz) (2t, 1H), 8.77-8.72 (m, 1H), 7.98 (dd, J=8.9, 1.6 Hz) and 7.92(dd, J=8.9, 1.6 Hz) (2dd, 1H), 7.70 (d) and 7.66 (d, J=8.9 Hz) (2d, 1H),7.55-6.90 (m, 8H), 5.73 and 5.56 (2s, 2H), 5.30-5.12 (m, 1H), 4.64-4.50and 4.29-4.21 (2m, 1H), 4.47 (d, J=5.6 Hz) and 4.32 (d, J=5.9 Hz) (2d,2H), 4.19 and 3.85 (2s, 2H), 2.69 and 2.64 (2s, 3H), 1.55-1.46 (m, 3H),1.25 (d, J=6.6 Hz) and 1.00 (d, J=6.7 Hz) (2d, 6H); ¹⁹F NMR (282 MHz,DMSO-d₆) δ −121.22, −121.73; MS (ES−): 604.2 (M−1).

Preparation of2-(3-acetyl-5-(pyrimidin-2-ylethynyl)-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(226a)

Reaction of2-(3-acetyl-5-bromo-1H-indazol-1-yl)-N-(2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)-N-isopropylacetamide(156f) (300 mg, 0.56 mmol) using Cs₂CO₃ (365 mg, 1.12 mmol),dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine (X-PHOS, 53mg, 0.112 mmol), Pd₂(dba)₃ (51 mg, 0.056 mmol) according to procedurereported in Scheme 92 gave after workup and purification by flash columnchromatography [silica gel (12 g), eluting with MeOH in DCM from 0 to100%]2-(3-acetyl-5-(pyrimidin-2-ylethynyl)-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(226a) (16 mg, 0.029 mmol, 5% yield) as a dark-yellow solid as a mixtureof two rotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 8.93-8.80 (m) and 8.36 (t,J=5.8 Hz) (3H), 8.49-8.42 (m, 1H), 7.82-6.98 (m, 6H), 5.76 & 5.59 (2s,2H), 4.64-4.52 & 4.29-4.21 (2m, 1H), 4.48 (d, J=5.6 Hz) & 4.32 (d, J=5.8Hz) (2d, 2H), 4.19 & 3.85 (2s, 2H), 2.64 (s, 3H), 1.26 (d, J=6.4 Hz) &1.00 (d, J=6.8 Hz (2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.20,−121.71; MS (ES+): 561.5 (M+1), 583.5 (M+Na); MS (ES−): 559.4 (M−1),595.4 (M+Cl).

Preparation of methyl3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylate(227a)

Reaction of 2-(3-acetyl-5-(methoxycarbonyl)-1H-indazol-1-yl)acetic acid(206c) TFA adduct (2.09 g, 5.36 mmol) withN-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide (10b) (1.65 g,6.43 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column [silica (40 g),eluting with DMA80 in DCM 0 to 40%] methyl3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylate(227a) (2.3 g, 4.47 mmol, 83% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.87-8.81 (m, 1H), 8.48 (t, J=5.9 Hz, 1H), 7.99 (dd, J=8.9,1.6 Hz, 1H), 7.88-7.77 (m, 1H), 7.50-7.39 (m, 1H), 7.28-7.18 (m, 1H),7.14-7.03 (m, 1H), 5.80 (s, 2H), 4.34 (d, J=5.7 Hz, 2H), 3.99 (s, 2H),3.91 (s, 3H), 3.20-3.05 (m, 1H), 2.65 (s, 3H), 1.10-0.99 (m, 2H),0.96-0.82 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.57; MS (ES+): 515.5(M+1); MS (ES−); 513.4 (M−1).

Preparation of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (228a)

Reaction of methyl3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylate(227a) (2.3 g, 4.47 mmol) in MeOH (25 mL) and water (25 mL) with asolution of lithium hydroxide hydrate (1.31 g, 31.3 mmol) in water (10mL) according to the procedure reported in step-2 of Scheme 129 gaveafter workup3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (228a) (2.2 g, 4.39 mmol, 98% yield) as a white solid; ¹H NMR (300MHz, DMSO-d₆) δ 13.05 (s, 1H), 8.88-8.80 (m, 1H), 8.50 (t, J=5.9 Hz,1H), 8.04-7.95 (m, 1H), 7.84-7.75 (m, 1H), 7.51-7.40 (m, 1H), 7.29-7.19(m, 1H), 7.14-7.04 (m, 1H), 5.80 (s, 2H), 4.34 (d, J=5.7 Hz, 2H), 4.00(s, 2H), 3.20-3.07 (m, 1H), 2.65 (s, 3H), 1.09-0.99 (m, 2H), 0.98-0.83(m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.57; MS (ES+): 501.5 (M+1);(ES−): 499.4 (M−1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(pyrimidin-2-yloxy)-1H-indazole-3-carboxamide(229c) Step-1: Preparation of tert-butyl2-(3-carbamoyl-5-(pyrimidin-2-yloxy)-1H-indazol-1-yl)acetate (229a)

To a solution of tert-butyl2-(3-carbamoyl-5-hydroxy-1H-indazol-1-yl)acetate (214b) (115 mg, 0.4mmol) in acetonitrile (5 mL) was added 2-bromopyrimidine (78 mg, 0.49mmol), potassium carbonate (164 mg, 1.18 mmol) and heated at reflux for16 h. The reaction mixture was concentrated in vacuum and residue wassuspended in brine (50 mL) and extracted with EtOAc (2×50 mL). Theorganic layers were combined dried, filtered and evaporated to dryness.The residue was purified by flash column chromatography [silica gel (12g), eluting with EtOAc/MeOH (9:1) in hexanes from 0 to 100%] to affordtert-butyl 2-(3-carbamoyl-5-(pyrimidin-2-yloxy)-1H-indazol-1-yl)acetate(229a) (130 mg, 0.35 mmol, 89% yield) as an orange solid; ¹H NMR (300MHz, DMSO-d₆) δ 8.65 (s, 1H), 8.64 (s, 1H), 7.86 (dd, J=2.3, 0.7 Hz,1H), 7.81-7.75 (m, 2H), 7.46 (s, 1H), 7.34 (dd, J=9.0, 2.3 Hz, 1H), 7.28(t, J=4.8 Hz, 1H), 5.39 (s, 2H), 1.44 (s, 9H); MS (ES+): 370.4 (M+1),739.7 (2M+1), 392.4 (M+Na); MS (ES−): 368.4 (M−1).

Step-2: Preparation of2-(3-carbamoyl-5-(pyrimidin-2-yloxy)-1H-indazol-1-yl)acetic acid (229b)

Reaction of tert-butyl2-(3-carbamoyl-5-(pyrimidin-2-yloxy)-1H-indazol-1-yl)acetate (229a) (118mg, 0.32 mmol) with TFA (0.74 mL, 9.58 mmol) in DCM (5 mL) according tothe procedure reported in step-2 of Scheme 2 gave after workup andtrituration with hexanes,2-(3-carbamoyl-5-(pyrimidin-2-yloxy)-1H-indazol-1-yl)acetic acid (229b)(0.129 g, 0.302 mmol, 95% yield) as a yellow solid in the form of TFAadduct; MS (ES+): 314.3 (M+1).

Step-3: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(pyrimidin-2-yloxy)-1H-indazole-3-carboxamide(229c)

Reaction of 2-(3-carbamoyl-5-(pyrimidin-2-yloxy)-1H-indazol-1-yl)aceticacid (229b) TFA adduct (119 mg, 0.38 mmol withN-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide (19c) (118 mg,0.46 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column [silica (12 g),eluting with MeOH in DCM, 0 to 50%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(pyrimidin-2-yloxy)-1H-indazole-3-carboxamide(229c) (85 mg, 0.15 mmol, 40% yield) as an off-white solid as a mixtureof two rotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 8.83 (t, J=5.7 Hz) & 8.38(t, J=5.9 Hz) (2t, 1H), 8.67-8.62 (m, 2H), 7.88-7.83 (m, 1H), 7.75 and7.73 (2s, 1H), 7.68 (dd, J=9.1, 0.7 Hz) and 7.62 (dd, J=9.1, 0.7 Hz)(2dd, 1H), 7.55-7.01 (m, 6H), 5.63 & 5.49 (2s, 2H), 4.65-4.50 &4.39-4.24 (2m, 1H), 4.46 (d, J=5.6 Hz) & 4.32 (d, J=5.8 Hz) (2d, 2H),4.19 & 3.85 (2s, 2H), 1.24 (d, J=6.4 Hz) & 1.00 (d, J=6.7 Hz) (2d, 6H);¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.21, −121.77; MS (ES+): 554.5 (M+1),576.5 (M+Na); MS (ES−): 588.4 (M+Cl).

Preparation of1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(3,3-difluoropiperidine-1-carboxamido)-1H-indazole-3-carboxamide(230c) Step-1: Preparation of methyl3-carbamoyl-1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylate(230a)

Reaction of 2-(3-carbamoyl-5-(methoxycarbonyl)-1H-indazol-1-yl)aceticacid (132f) TFA adduct (300 g, 0.94 mmol) withN-(2′-chloro-2-fluorobiphenyl-3-yl)-2-(isopropylamino)acetamide (115c)(300 mg, 0.94 mmol) according to the procedure reported in step-3 ofscheme-2 gave after workup and purification by flash column [silica(24g), eluting with DMA80 in DCM 0 to 20%] methyl3-carbamoyl-1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylate(230a) (310 mg, 0.53 mmol, 57% yield) as an off-white solid; ¹H NMR (300MHz, DMSO-d₆) (mixture of two rotamers) δ 10.27 and 9.76 (2s, 1H),8.91-8.86 (m, 1H), 8.16-6.96 (m, 11H), 5.71 and 5.56 (2s, 2H), 4.68-4.55and 4.38-4.26 (2m, 1H), 4.47 and 4.08 (2s, 2H), 3.909 and 3.90 (2s, 3H),1.27 and 1.06 (2d, J=6.8 Hz, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −126.77,−126.94; MS (ES+): 580.5 (M+1), 602.5 (M+Na), MS (ES−): 578.5 (M−1),614.6 (M+Cl).

Step-2: Preparation3-carbamoyl-1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (230b)

Reaction of methyl3-carbamoyl-1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylate(230a) (300 mg, 0.52 mmol) in THF (5 mL) with a solution of lithiumhydroxide hydrate (25 mg, 1.03 mmol) in water (1 mL) according to theprocedure reported in step-2 of scheme-29 gave after workup3-carbamoyl-1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (230b) (270 mg, 0.48 mmol, 92% yield) as a white solid; ¹H NMR (300MHz, DMSO-d₆) (mixture of two rotamers) δ 12.94 (s, 1H), 10.26 and 9.76(2s, 1H), 8.86 and 8.85 (2dd, J=1.6, 0.8 Hz, 1H), 8.16-6.96 (m, 11H),5.69 and 5.55 (2s, 2H), 4.68-4.56 and 4.37-4.28 (m, 1H), 4.47 and 4.08(2s, 2H), 1.27 and 1.06 (2d, J=6.8 Hz, 6H); MS (ES−): 564.4 & 566.4(M−1).

Step-3: Preparation of1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(3,3-difluoropiperidine-1-carboxamido)-1H-indazole-3-carboxamide(230c)

Compound 230c was prepared from3-carbamoyl-1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (230b) (150 mg, 0.27 mmol) according to the procedure reported instep-3 of scheme-223. This gave after work up and purification by flashcolumn chromatography [silica gel (12 g), eluting with MeOH:EtOAc (9:1)in hexanes 0 to 70%] (120 mg, 0.18 mmol, 66% yield) of compound 230c aswhite solid; ¹H NMR (300 MHz, DMSO-d₆) (mixture of two rotamers) δ 10.25and 9.77 (2s, 1H), 8.78 and 8.77 (2s, 1H), 8.188 and 8.183 (2s, 1H),8.19-8.05 and 7.99-7.90 (2m, 1H), 7.69-6.99 (m, 10H), 5.58 and 5.45 (2s,2H), 4.70-4.56 and 4.38-4.27 (2m, 1H), 4.46 and 4.08 (2s, 2H), 3.81 (t,J=12.1 Hz, 2H), 3.58-3.47 (m, 2H), 2.18-1.95 (m, 2H), 1.79-1.64 (m, 2H),1.25 and 1.06 (2d, J=6.8 Hz, 6H); 19F NMR (282 MHz, DMSO-d₆) (mixture oftwo rotamers) δ −101.16, −126.79 and −126.98; MS (ES+): 684.6 (M+1).

Preparation of2-(1-acetyl-1H-indol-3-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(231c) Step-1: Preparation ofN-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-2-(1H-indol-3-yl)-N-isopropylacetamide(231b)

Reaction of N-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide(19c) (795 mg, 3.07 mmol) with 2-(1H-indol-3-yl)acetic acid (231a) (359mg, 2.05 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and trituration of crude with EtOAcN-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-2-(1H-indol-3-yl)-N-isopropylacetamide(231b) (583 mg, 1.40 mmol, 68% yield) as a white solid as a mixture oftwo rotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 10.89 (s, 1H), 8.63 (t, J=5.7Hz) & 8.32 (t, J=5.9 Hz) (2t, 1H), 7.58-6.90 (m, 8H), 4.73-4.57 &4.29-4.16 (2m, 1H), 4.41 (d, J=5.7 Hz) & 4.34 (d, J=5.9 Hz) (2d, 2H),3.94 & 3.60 (2s, 2H), 3.81 & 3.80 (2s, 2H), 1.00 (d, J=6.5 Hz) & 0.96(d, J=6.8 Hz) (2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.31, −121.81;MS (ES+): 416.5 (M+1), 438.5 (M+Na); MS (ES−): 414.4 (M−1), 450.4(M+Cl).

Step-2: Preparation of2-(1-acetyl-1H-indol-3-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(231c)

To a solution ofN-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-2-(1H-indol-3-yl)-N-isopropylacetamide(231b) (0.15 g, 0.360 mmol) in THF (5 mL) at 0° C. under Argonatmosphere was added potassium tert-butoxide (40 mg, 0.361 mmol) andstirred for 10 mins. To the resulting suspension was added acetylchloride (0.023 mL, 0.325 mmol) and stirred at 0° C. for 30 mins. Thereaction mixture quenched with saturated aqueous NH₄C₁ solution (30 mL)and extracted with EtOAc (2×30 mL). The combined organic layers werewashed with brine, dried, filtered and concentrated in vacuum. Theresidue obtained was purified by flash column chromatography [silica gel(12 g), eluting with EtOAc in hexanes o to 100%] to afford2-(1-acetyl-1H-indol-3-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(231c) (42 mg, 0.092 mmol, 25% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) (mixture of two rotamers) δ 8.70 and 8.40 (2t, J=5.9 Hz, 1H),8.33-8.27 (m, 1H), 7.90 and 7.63 (2s, 1H), 7.61-7.09 (m, 6H), 4.71-4.59and 4.29-4.18 (2m, 1H), 4.42 and 4.35 (2d, J=5.8 Hz, 2H), 4.09 and 3.69(2s, 2H), 3.85 (s, 2H), 2.60 and 2.59 (2s, 3H), 1.10 (d, J=6.5 Hz) and0.99 (d, J=6.8 Hz) (2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) (a mixture oftwo rotamers) δ −121.29, −121.75; MS (ES+) 480.4 & 482.5 (M+Na); MS(ES−): 456.4 & 458.4 (M−1).

Preparation of2-(1-acetyl-1H-indazol-3-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(232c) Step-1: Preparation ofN-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-2-(1H-indazol-3-yl)-N-isopropylacetamide(232b)

Reaction of N-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide(19c) (257 mg, 0.99 mmol) with 2-(1H-indazol-3-yl)acetic acid (232a)(175 mg, 0.99 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup and purification by flash columnchromatography [silica gel (12 g), eluting with EtOAc in hexane 0 to100%]N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-2-(1H-indazol-3-yl)-N-isopropylacetamide(232b) (310 mg, 0.74 mmol, 75% yield); ¹H NMR (300 MHz, DMSO-d₆) (amixture of two rotamers) δ 12.85 and 12.76 (2s, 1H), 8.70 and 8.48 (2t,J=6.0 Hz, 1H), 7.70 and 7.65 (2d, J=8.1 Hz, 1H), 7.54-6.99 (m, 6H),4.68-4.57 and 4.33-4.23 (2m, 1H), 4.42 and 4.37 (2d, J=6.0 Hz, 2H), 4.11and 4.09 (2s, 2H), 3.90 and 3.81 (2s, 2H), 1.03 and 0.95 (2d, J=6.8 Hz,6H); MS (ES+): 417.4 (M+1), 439.4 (M+Na): MS (ES−): 415.3 (M−1).

Step-2: Preparation of2-(1-acetyl-1H-indazol-3-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(232c)

To a solution ofN-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-2-(1H-indazol-3-yl)-N-isopropylacetamide(232b) (150 mg, 0.36 mmol) in DCM (5 mL) was added at room temperaturetriethylamine (0.15 mL, 1.08 mmol), DMAP (8.79 mg, 0.072 mmol), aceticanhydride (0.068 mL, 0.72 mmol) and stirred at RT for 48h. The reactionmixture was concentrated to dryness and purified by flash columnchromatography [silica gel (12 g), eluting with EtOAc in hexane 0 to100%] to afford2-(1-acetyl-1H-indazol-3-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(232c) (82 mg, 0.18 mmol, 50% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) (mixture of two rotamers) δ 8.75 and 8.34 (2t, J=5.7 Hz, 1H),8.30 and 8.27 (2dt, J=2.7, 0.9 Hz, 1H), 7.82-7.74 (m, 1H), 7.64-7.57 (m,1H), 7.52-7.02 (m, 4H), 4.69-4.57 and 4.40-4.36 (2m, 1H), 4.43 and 4.33(2d, J=6.0 Hz, 2H), 4.24 and 4.15 (2s, 2H), 4.05 and 3.83 (2s, 2H), 2.68and 2.67 (2s, 3H), 1.17 and 1.00 (2d, J=6.8 Hz, 6H); ¹⁹FNMR (282 MHz,DMSO-d₆) (a mixture of two rotamers) δ −121.28, −121.81; MS (ES+) 459.5(M+1), 481.4 (M+23), MS (ES−) 493.4 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-N5-(pyridin-4-ylmethyl)-1H-indazole-3,5-dicarboxamide(233a)

Reaction of3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (144a) (50 mg, 0.1 mmol) with pyridin-4-ylmethanamine (0.015 mL,0.15 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column chromatography[silica (4 g), eluting with MeOH in DCM (1:0 to 9:1)]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-N5-(pyridin-4-ylmethyl)-1H-indazole-3,5-dicarboxamide(233a) (26 mg, 44%) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) (mixtureof two rotamers) δ 9.32-9.26 (m, 1H), 8.83 (t, J=5.9 Hz) and 8.36 (t,J=5.9 Hz) (2t, 1H), 8.80-8.77 (m, 1H), 8.53-8.47 (m, 2H), 7.94 (ddd,J=10.8, 8.9, 1.7 Hz, 1H), 7.83 and 7.80 (2s, 1H), 7.72-7.60 (m, 1H),7.56-6.95 (m, 6H), 5.64 and 5.50 (2s, 2H), 4.62-4.22 (m, 5H), 4.19 and3.84 (2s, 2H), 1.23 (d, J=6.4 Hz) and 0.99 (d, J=6.8 Hz) (2d, 6H); ¹⁹FNMR (282 MHz, DMSO-d₆) δ −121.22, −121.72; MS (ES+): 594.6 & 596.6(M+1); MS (ES−): 628.6 & 630.5 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((1s,4s)-4-hydroxycyclohexyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(234b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-(((cis)-4-hydroxycyclohexyl)amino)acetamide(234a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (500 mg,2.12 mmol) with (1s,4s)-4-aminocyclohexanol (244 mg, 2.12 mmol)according to the procedure reported in step-2 of Scheme 35 gave afterworkupN-(3-chloro-2-fluorobenzyl)-2-(((cis)-4-hydroxycyclohexyl)amino)acetamide(234a) as a colorless oil which was used as such in the next step; MS(ES+): 315.4 (M+1); MS (ES−): 313.4 (M−1).

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((cis)-4-hydroxycyclohexyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(234b)

Reaction of N-(3-chloro-2-fluorobenzyl)-2-(((1 s,4s)-4-hydroxy cyclohexyl)amino)acetamide (234a) (360 mg, 1.14 mmol) with2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e) (301 mg, 1.37 mmol)according to the procedure reported in step-3 of Scheme 2 gave afterworkup1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((cis)-4-hydroxycyclohexyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(234b) (163 mg, 0.32 mmol, 28% yield) as a white solid as a mixture oftwo rotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 8.89 (t, J=5.7 Hz) & 8.36 (t,J=6.0 Hz) (2t, 1H), 8.23-8.11 (m, 1H), 7.79-6.98 (m, 8H), 5.61 & 5.45(2s, 2H), 4.52-3.73 (m, 7H), 1.88-1.13 (m, 8H); ¹⁹F NMR (282 MHz,DMSO-d₆) δ −121.25, −121.69; MS (ES+): 516.5 (M+1), 538.4 (M+Na); MS(ES−): 514.4 (M−1), 550.5 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(3,3-difluoropiperidine-1-carboxamido)-1H-indazole-3-carboxamide(235b) Step-1: Preparation of3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (235a)

Compound 235a was prepared from3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (199a) (4 g, 7.97 mmol) according to the procedure reported instep-3 of Scheme 129 to afford product as a white solid (6.6 g, 12.53mmol, 157% yield), which was used in the next step without furtherpurification; MS (ES−): 525.4 (M−1).

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(3,3-difluoropiperidine-1-carboxamido)-1H-indazole-3-carboxamide(235b)

Compound 235b was prepared from3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (235a) (500 mg, 0.47 mmol) and 3,3-difluoropiperidinehydrochloride (150 mg, 0.95 mmol) using TEA (0.27 mL, 1.9 mmol) as baseaccording to the procedure reported in step-4 of Scheme 129 to affordafter workup and purification by column chromatography [silica gel (12g), eluting with DMA80 in DCM 0 to 40%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(3,3-difluoropiperidine-1-carboxamido)-1H-indazole-3-carboxamide(235b) (86 mg, 0.14 mmol, 29% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.78 (s, 1H), 8.50 (t, J=5.8 Hz, 1H), 8.25-8.13 (m, 1H), 7.65(s, 1H), 7.59-7.42 (m, 3H), 7.33 (s, 1H), 7.28-7.19 (m, 1H), 7.17-7.08(m, 1H), 5.61 (s, 2H), 4.33 (d, J=5.7 Hz, 2H), 3.99 (s, 2H), 3.82 (t,J=12.0 Hz, 2H), 3.60-3.46 (m, 2H), 3.13-2.94 (m, 1H), 2.18-1.96 (m, 2H),1.81-1.63 (m, 2H), 1.04-0.84 (m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−101.17, −121.60; MS (ES⁺): 620.6 (M+1); MS (ES⁻): 618.5 (M−1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-6-(3,3-difluoropiperidine-1-carboxamido)-1H-indazole-3-carboxamide(236b) Step-1: Preparation of3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-6-carbonylazide (236a)

Compound 236a was prepared from3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-6-carboxylicacid (208a) (800 mg, 1.6 mmol) according to the procedure reported instep-3 of Scheme 129 to afford product; MS (ES+) 549.5 (M+Na).

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-6-(3,3-difluoropiperidine-1-carboxamido)-1H-indazole-3-carboxamide(236b)

Compound 236b was prepared from3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-6-carbonylazide (236a) (200 mg, 0.38 mmol) and 3,3-difluoropiperidinehydrochloride (120 mg, 0.76 mmol) using TEA (0.21 mL, 1.51 mmol) as baseaccording to the procedure reported in step-4 of Scheme 129 to affordafter workup and purification by column chromatography [silica gel (12g), eluting with DMA80 in DCM 0 to 40%] (26 mg, 0.042 mmol, 11.05%yield) product as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 8.93 (s,1H), 8.58 (t, J=5.8 Hz, 1H), 8.01 (d, J=8.6 Hz, 1H), 7.77 (s, 1H),7.74-7.61 (m, 1H), 7.49-7.43 (m, 1H), 7.36-7.31 (m, 2H), 7.27-7.21 (m,1H), 7.17-7.12 (m, 1H), 5.57 (s, 2H), 4.33 (d, J=5.5 Hz, 2H), 4.00 (s,2H), 3.82 (t, J=11.9 Hz, 2H), 3.55-3.51 (m, 2H), 3.15-2.97 (m, 1H),2.13-1.97 (m, 2H), 1.81-1.64 (m, 2H), 1.34-1.20 (m, 2H), 1.00-0.92 (m,2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −101.18, −121.66; MS (ES+) 620.6(M+1); MS (ES−): 654.5, 656.5 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(4-cyclopropylpiperazine-1-carboxamido)-1H-indazole-3-carboxamide(237a)

Compound 237a was prepared from3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (235a) (200 mg, 0.19 mmol) and 1-cyclopropylpiperazine (48 mg,0.38 mmol) using TEA (0.11 mL, 0.76 mmol) as base according to theprocedure reported in step-4 of Scheme 129. This gave after workup andpurification by flash column chromatography [silica gel (12 g), elutingwith DMA80 in DCM 0 to 40%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(4-cyclopropylpiperazine-1-carboxamido)-1H-indazole-3-carboxamide(237a) (30 mg, 0.048 mmol, 25% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.65 (s, 1H), 8.50 (t, J=5.9 Hz, 1H), 8.21-8.15 (m, 1H),7.67-7.60 (m, 1H), 7.60-7.42 (m, 3H), 7.35-7.28 (m, 1H), 7.27-7.20 (m,1H), 7.18-7.09 (m, 1H), 5.61 (s, 2H), 4.33 (d, J=5.7 Hz, 2H), 3.99 (s,2H), 3.42 (t, J=4.9 Hz, 4H), 3.10-3.01 (m, 1H), 2.58-2.52 (m, 4H),1.71-1.61 (m, 1H), 1.02-0.96 (m, 2H), 0.95-0.89 (m, 2H), 0.46-0.40 (m,2H), 0.38-0.33 (m, 2H); ¹⁹F NMR (282 MHz, DMSO) δ −121.60; MS (ES+)625.7 (M+1), 647.7 (M+Na); (ES−) 623.6 (M−1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(3-(2-(diethylamino)ethyl)ureido)-1H-indazole-3-carboxamide(238a)

Compound 238a was prepared from3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (235a) (150 mg, 0.14 mmol) and N¹,N¹-diethylethane-1,2-diamine (33mg, 0.29 mmol) using TEA (0.08 mL, 0.57 mmol) as base according to theprocedure reported in step-4 of Scheme 129. This gave after workup,purification by flash column chromatography [silica gel (12 g), elutingwith DMA80 in DCM 0 to 40%] and prep-HPLC [eluting with CH₃CN in water(contains 0.1% TFA) from 0-100%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(3-(2-(diethylamino)ethyl)ureido)-1H-indazole-3-carboxamide(238a) (16 mg, 0.026 mmol, 18% yield) as an off white solid; ¹H NMR (300MHz, DMSO-d₆) δ 8.81 (s, 1H), 8.50 (t, J=5.9 Hz, 1H), 8.24-8.13 (m, 1H),7.60 (s, 1H), 7.53-7.41 (m, 3H), 7.33-7.27 (m, 1H), 7.27-7.19 (m, 1H),7.17-7.07 (m, 1H), 6.00 (t, J=5.4 Hz, 1H), 5.60 (s, 2H), 4.33 (d, J=5.7Hz, 2H), 3.98 (s, 2H), 3.16 (q, J=6.2 Hz, 2H), 3.09-2.95 (m, 1H),2.57-2.50 (m, 6H), 1.07-0.83 (m, 10H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−73.45 (TFA peak), −121.60; MS (ES+) 615.7 (M+1); MS (ES−): 614.6 (M−1).

Preparation ofN-(3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazol-5-yl)-3,3-difluoropiperidine-1-carboxamide(239b) Step-1: Preparation of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (239a)

Compound 235a was prepared from3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (228a) (630 mg, 1.26 mmol) according to the procedure reported instep-3 of Scheme 129 to afford product as a white solid (750 mg, 1.426mmol, 113% yield), which was used in the next step without furtherpurification. MS (ES+): 526.5 (M+1).

Step-2: Preparation ofN-(3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazol-5-yl)-3,3-difluoropiperidine-1-carboxamide(239b)

Compound 239b was prepared from3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (239a) (350 mg, 0.67 mmol) and 3,3-difluoropiperidinehydrochloride (210 mg, 1.33 mmol) using TEA (0.37 mL, 2.66 mmol) as baseaccording to the procedure reported in step-4 of Scheme 129. This gaveafter workup and purification by flash column chromatography [silica gel(12 g), eluting with DMA80 in DCM 0 to 40%]N-(3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazol-5-yl)-3,3-difluoropiperidine-1-carboxamide(239b) (190 mg, 0.31 mmol, 46% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.83 (s, 1H), 8.48 (t, J=5.8 Hz, 1H), 8.28-8.19 (m, 1H),7.63-7.52 (m, 2H), 7.45 (td, J=7.6, 1.7 Hz, 1H), 7.23 (td, J=7.3, 6.8,1.7 Hz, 1H), 7.15-7.07 (m, 1H), 5.70 (s, 2H), 4.34 (d, J=5.7 Hz, 2H),3.99 (s, 2H), 3.82 (t, J=12.0 Hz, 2H), 3.61-3.47 (m, 2H), 3.19-3.01 (m,1H), 2.60 (s, 3H), 2.17-1.97 (m, 2H), 1.80-1.64 (m, 2H), 1.07-0.96 (m,2H), 0.96-0.80 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −101.17, −121.61;MS (ES+) 619.7 (M+1); (ES−): 617.6 (M−1).

Preparation of2-(3-acetyl-5-amino-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(240f) Step-1: Preparation of ethyl2-(3-iodo-5-nitro-1H-indazol-1-yl)acetate (240b)

Reaction of 3-iodo-5-nitro-1H-indazole (240a) (3 g, 10.38 mmol) withethyl 2-bromoacetate (1.38 mL, 12.46 mmol) using sodium hydride (0.46 g,11.42 mmol) as base according to the procedure reported in step-1 ofScheme 57 gave after workup and purification by flash columnchromatography [silica (40 g), eluting with EtOAc in hexane 0 to 30%]ethyl 2-(3-iodo-5-nitro-1H-indazol-1-yl)acetate (240b) (2.52 g, 6.72mmol, 64.7% yield) as an orange solid; ¹H NMR (300 MHz, DMSO-d₆) δ8.38-8.30 (m, 2H), 7.95 (d, J=9.9 Hz, 1H), 5.56 (s, 2H), 4.16 (q, J=7.1Hz, 2H), 1.21 (t, J=7.1 Hz, 3H); MS (ES+): 376.3 (M+1), 398.3 (M+Na).

Step-2: Preparation of ethyl 2-(3-acetyl-5-nitro-1H-indazol-1-yl)acetate(240c)

Reaction of ethyl 2-(3-iodo-5-nitro-1H-indazol-1-yl)acetate (240b) (1.5g, 4.00 mmol) in Toluene (40 mL) using tributyl(1-ethoxyvinyl)stannane(1.62 mL, 4.80 mmol) and Pd(PPh₃)₄ according to the procedure reportedin step-1 and step-2 of Scheme 206 gave after workup and purification byflash column chromatography [silica gel (24 g), eluting with EtOAc inDCM 0 to 20%] ethyl 2-(3-acetyl-5-nitro-1H-indazol-1-yl)acetate (240c)(0.83 g, 2.85 mmol, 71% yield) as dark orange solid; ¹H NMR (300 MHz,DMSO-d₆) δ 9.01 (dd, J=2.3, 0.7 Hz, 1H), 8.37 (dd, J=9.3, 2.2 Hz, 1H),8.06 (dd, J=9.3, 0.7 Hz, 1H), 5.70 (s, 2H), 4.19 (q, J=7.1 Hz, 2H), 2.67(s, 3H), 1.22 (t, J=7.1 Hz, 3H); MS (ES+): 292.3 (M+1), MS (ES−): 326.3(M+Cl).

Step-3: Preparation of 2-(3-acetyl-5-nitro-1H-indazol-1-yl)acetic acid(240d)

Reaction of ethyl 2-(3-acetyl-5-nitro-1H-indazol-1-yl)acetate (240c)(0.8 g, 2.75 mmol) in THF (20 mL) using a solution of lithium hydroxidehydrate (0.13 g, 5.49 mmol) in water (5 mL) according to the procedurereported in step-2 of Scheme 129 gave after workup2-(3-acetyl-5-nitro-1H-indazol-1-yl)acetic acid (240d) (0.71 g, 2.7mmol, 98% yield) as off-white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 13.52(s, 1H), 9.00 (dd, J=2.2, 0.6 Hz, 1H), 8.36 (dd, J=9.3, 2.2 Hz, 1H),8.06 (dd, J=9.4, 0.7 Hz, 1H), 5.58 (s, 2H), 2.67 (s, 3H); MS (ES+):264.3 (M+1); MS (ES−): 262.2 (M−1).

Step-4: Preparation of2-(3-acetyl-5-nitro-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(240e)

Reaction of 2-(3-acetyl-5-nitro-1H-indazol-1-yl)acetic acid (240d) (0.65g, 2.47 mmol) withN-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide (10b) (0.7 g,2.72 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column [silica (12 g),eluting with DMA80 in DCM 0 to 40%]2-(3-acetyl-5-nitro-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(240e) (820 mg, 1.63 mmol, 66% yield) as a light orange solid; ¹H NMR(300 MHz, DMSO-d₆) δ 9.00 (dd, J=2.3, 0.6 Hz, 1H), 8.49 (t, J=5.9 Hz,1H), 8.30 (dd, J=9.3, 2.2 Hz, 1H), 7.95 (dd, J=9.3, 0.7 Hz, 1H), 7.45(td, J=7.6, 1.7 Hz, 1H), 7.26-7.17 (m, 1H), 7.09 (td, J=7.9, 1.0 Hz,1H), 5.87 (s, 2H), 4.34 (d, J=5.7 Hz, 2H), 3.99 (s, 2H), 3.19-3.07 (m,1H), 2.67 (s, 3H), 1.09-0.99 (m, 2H), 0.96-0.86 (m, 2H); ¹⁹F NMR (282MHz, DMSO-d₆) δ −121.56; MS (ES+): 524.4 (M+Na), MS (ES−): 536.3 (M+Cl).

Step-5: Preparation of2-(3-acetyl-5-amino-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(240f)

To a solution of2-(3-acetyl-5-nitro-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(240e) (800 mg, 1.59 mmol) in THF (20 mL) and MeOH (5 mL) was addedNH₄C₁ (1.71 g, 31.9 mmol), Zinc (1.04 g, 15.94 mmol) and stirred at RTfor 3 h. The reaction mixture was filtered over a Celite pad, washedwith 20% MeOH in EtOAc (2×8 mL). The filtrate was concentrated in vacuumto dryness and the resultant residue was suspended in brine (60 mL) andEtOAc (80 mL). The organic layer was separated dried, filtered andconcentrated in vacuum to afford2-(3-acetyl-5-amino-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(240f) (650 mg, 1.378 mmol, 86% yield) as a light orange solid; ¹H NMR(300 MHz, DMSO-d₆) δ 8.47 (t, J=5.4 Hz, 1H), 7.53-7.41 (m, 1H), 7.35 (d,J=8.9 Hz, 1H), 7.30-7.07 (m, 3H), 6.81 (dd, J=8.9, 2.1 Hz, 1H), 5.60 (s,2H), 5.21 (s, 2H), 4.34 (d, J=5.8 Hz, 2H), 3.98 (s, 2H), 3.14-3.03 (m,1H), 2.53 (s, 3H), 1.04-0.95 (m, 2H), 0.93-0.84 (m, 2H); ¹⁹F NMR (282MHz, DMSO-d₆) δ −121.62; MS (ES+): 472.4 (M+1), 494.4 (M+Na), MS (ES−):506.4 (M+Cl).

Preparation ofN-(3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazol-5-yl)cyclohexanecarboxamide(241a)

Reaction of2-(3-acetyl-5-amino-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(240f) (100 mg, 0.21 mmol) with cyclohexanecarboxylic acid (33 mg, 0.25mmol) according to the procedure reported in step-3 of Scheme 2 gaveafter workup and purification by flash column chromatography [silica (12g), eluting with EtOAc in hexane 0 to 100%]N-(3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazol-5-yl)cyclohexanecarboxamide(241a) (85 mg, 0.15 mmol, 69% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 9.97 (s, 1H), 8.54-8.51 (m, 1H), 8.48 (t, J=5.9 Hz, 1H),7.67-7.56 (m, 2H), 7.50-7.42 (m, 1H), 7.27-7.17 (m, 1H), 7.10 (td,J=7.9, 1.0 Hz, 1H), 5.71 (s, 2H), 4.34 (d, J=5.8 Hz, 2H), 3.98 (s, 2H),3.18-3.04 (m, 1H), 2.60 (s, 3H), 2.41-2.28 (m, 1H), 1.91-1.58 (m, 6H),1.52-1.14 (m, 4H), 1.07-0.97 (m, 2H), 0.95-0.84 (m, 2H); ¹⁹F NMR (282MHz, DMSO-d₆) δ −121.60; MS (ES+): 604.6 (M+Na); MS (ES−): 580.5 (M−1),616.5 (M+Cl).

Preparation of2-(3-acetyl-5-(2-cyclopropylacetamido)-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(242a)

Reaction of2-(3-acetyl-5-amino-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(240f) (100 mg, 0.21 mmol) with 2-cyclopropylacetic acid (25 mg, 0.25mmol) according to the procedure reported in step-3 of Scheme 2 gaveafter workup and purification by flash column chromatography [silica (12g), eluting with EtOAc in hexane 0 to 100%]2-(3-acetyl-5-(2-cyclopropylacetamido)-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(242a) (80 g, 0.14 mmol, 68% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 9.98 (s, 1H), 8.56-8.43 (m, 2H), 7.68-7.57 (m, 2H), 7.50-7.42(m, 1H), 7.10 (td, J=7.9, 1.0 Hz, 1H), 7.15-7.06 (m, 1H), 5.72 (s, 2H),4.34 (d, J=5.8 Hz, 2H), 3.99 (s, 2H), 3.17-3.05 (m, 1H), 2.60 (s, 3H),2.23 (d, J=7.0 Hz, 2H), 1.14-0.97 (m, 3H), 0.96-0.85 (m, 2H), 0.55-0.44(m, 2H), 0.26-0.16 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.60; MS(ES+): 576.6 (M+Na); MS (ES−): 588.5 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclobutylmethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(243b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-((cyclobutylmethyl)amino)acetamide (243a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (243 mg,1.03 mmol) with cyclobutylmethanamine hydrochloride (250 mg, 2.056 mmol)according to the procedure reported in step-2 of Scheme 35 gave afterworkup and purification by flash column chromatography [silica (12 g),eluting with EtOAc/MeOH (9:1) in hexane 0 to 60%]N-(3-chloro-2-fluorobenzyl)-2-((cyclobutylmethyl)amino)acetamide (243a)(203 mg, 0.71 mmol, 69% yield) as a clear oil which was used as such inthe next step; MS (ES⁺) 285.4 (M+1); (ES⁻) 283.3 (M−1).

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclobutylmethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide (243b)

Reaction ofN-(3-chloro-2-fluorobenzyl)-2-((cyclobutylmethyl)amino)acetamide (243a)(109 mg, 0.38 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e)(92 mg, 0.42 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with DMA80 in DCM 0 to 40%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclobutylmethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide (243b) (48 mg, 0.1 mmol, 26% yield) asa white solid as a mixture of two rotamers; ¹H NMR (300 MHz, DMSO-d₆) δ8.83 (t, J=5.7 Hz) and 8.46 (t, J=5.8 Hz) (2t, 1H), 8.18 (d, J=8.1 Hz,1H), 7.79-7.65 (m, 1H), 7.58-7.05 (m, 7H), 5.57 and 5.46 2 (s, 2H), 4.45(d, J=5.5 Hz) and 4.33 (d, J=5.7 Hz) (2d, 2H), 4.22 and 3.92 (2s, 2H),3.53 and, 3.29 (2d, J=7.2 Hz, 2H), 2.73-2.60 and 2.47-2.32 (m, 1H),2.07-1.50 (m, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.18, −121.60; MS(ES⁺) 486.5 (M+1); (ES⁻) 484.5 (M−1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(pyrimidin-5-yloxy)-1H-indazole-3-carboxamide(244c) Step-1: Preparation of tert-butyl2-(3-carbamoyl-5-(pyrimidin-5-yloxy)-1H-indazol-1-yl)acetate (229a)

Reaction of tert-butyl 2-(3-carbamoyl-5-hydroxy-1H-indazol-1-yl)acetate(214b) (164 mg, 0.56 mmol) with 5-bromopyrimidine (107 mg, 0.68 mmol)using cesium carbonate (367 mg, 1.13 mmol), Pd₂(dba)₃ (26 mg, 0.03 mmol)and (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (Xantphos,33 mg, 0.06 mmol) according to the procedure reported in step-1 ofScheme 97 gave after workup and purification by flash columnchromatography [silica gel (12 g), eluting with methanol in DCM 0 to100%] tert-butyl2-(3-carbamoyl-5-(pyrimidin-5-yloxy)-1H-indazol-1-yl)acetate (229a) (39mg, 0.11 mmol, 19% yield) as an off-white solid; MS (ES+): 370.4 (M+1);MS (ES−): 368.3 (M−1).

Step-2: Preparation2-(3-carbamoyl-5-(pyrimidin-5-yloxy)-1H-indazol-1-yl)acetic acid (244b)

Reaction of tert-butyl2-(3-carbamoyl-5-(pyrimidin-5-yloxy)-1H-indazol-1-yl)acetate (244a) (39mg, 0.11 mmol) with TFA (0.24 mL, 3.17 mmol) in DCM (10 mL) according tothe procedure reported in step-2 of Scheme 2 gave after workup2-(3-carbamoyl-5-(pyrimidin-5-yloxy)-1H-indazol-1-yl)acetic acid (244b)(33 mg, 0.11 mmol, 100% yield) as a yellow solid in the form of TFAadduct; MS (ES+): 314.3 (M+1); MS (ES−): 312.3 (M−1).

Step-3: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(pyrimidin-5-yloxy)-1H-indazole-3-carboxamide(244c)

Reaction of 2-(3-carbamoyl-5-(pyrimidin-5-yloxy)-1H-indazol-1-yl)aceticacid (244b) TFA adduct (33 mg, 0.11 mmol withN-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide (19c) (33 mg,0.13 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column [silica (12 g),eluting with DMA-80 in DCM, 0 to 100%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(pyrimidin-5-yloxy)-1H-indazole-3-carboxamide(244c) (8 mg, 0.014 mmol, 14% yield) as an off-white solid as a mixtureof two rotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 10.83 & 10.78 (2s, 1H),9.57 & 9.56 (2s, 1H), 9.29 & 9.28 (2s, 2H), 8.91 & 8.90 (2s, 1H), 8.85(t, J=5.8 Hz) & 8.40 (t, J=5.9 Hz) (2t, 1H), 7.60-6.94 (m, 6H), 5.62 &5.50 (2s, 2H), 4.63-3.78 (m, 5H), 1.23 (d, J=6.1 Hz) & 0.99 (d, J=6.8Hz) (2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.20, −121.69; MS (ES+):554.5 (M+1), 576.5 (M+Na); MS (ES−): 552.5 (M−1), 588.5 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(3-(pyridin-4-yl)ureido)-1H-indazole-3-carboxamide(245a)

Compound 245a was prepared from3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (235a) (300 mg, 0.29 mmol) and pyridin-4-amine (53.6 mg, 0.569mmol) using TEA (0.16 mL, 1.14 mmol) as base according to the procedurereported in step-4 of Scheme 129. This gave after workup, purificationby flash column chromatography [silica gel (12 g), eluting with DMA80 inDCM 0 to 40%] and prep-HPLC [eluting with CH₃CN in water (contains 0.1%TFA) from 0-100%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(3-(pyridin-4-yl)ureido)-1H-indazole-3-carboxamide(245a) (9 mg, 0.015 mmol, 5% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 10.75 (s, 1H), 9.87 (s, 1H), 8.60 (d, J=6.8 Hz, 2H), 8.51 (t,J=5.9 Hz, 1H), 8.44 (d, J=1.9 Hz, 1H), 7.94 (d, J=6.6 Hz, 2H), 7.73-7.68(m, 1H), 7.62 (d, J=9.0 Hz, 1H), 7.51-7.41 (m, 2H), 7.40-7.31 (m, 1H),7.30-7.19 (m, 1H), 7.18-7.06 (m, 1H), 5.65 (s, 2H), 4.33 (d, J=5.7 Hz,2H), 3.99 (s, 2H), 3.13-2.97 (m, 1H), 1.08-0.95 (m, 2H), 0.95-0.82 (m,2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −73.66 (TFA peak), −121.58; MS (ES+):593.5 (M+1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(3-cyclohexylureido)-1H-indazole-3-carboxamide(246a)

Compound 246a was prepared from3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (235a) (300 mg, 0.29 mmol) and cyclohexanamine (57 mg, 0.57 mmol)using TEA (0.16 mL, 1.14 mmol) as base according to the procedurereported in step-4 of Scheme 129. This gave after workup, purificationby flash column chromatography [silica gel (12 g), eluting with DMA80 inDCM 0 to 40%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(3-cyclohexylureido)-1H-indazole-3-carboxamide(246a) (15 mg, 0.025 mmol, 9% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.50 (t, J=6.0 Hz, 1H), 8.42 (s, 1H), 8.24-8.12 (m, 1H), 7.60(s, 1H), 7.55-7.37 (m, 3H), 7.30 (s, 1H), 7.26-7.18 (m, 1H), 7.12 (t,J=7.8 Hz, 1H), 5.99 (d, J=7.8 Hz, 1H), 5.60 (s, 2H), 4.33 (d, J=5.8 Hz,2H), 3.98 (s, 2H), 3.58-3.42 (m, 1H), 3.14-2.97 (m, 1H), 1.93-1.75 (m,2H), 1.75-1.61 (m, 2H), 1.61-1.44 (m, 1H), 1.36-1.13 (m, 5H), 1.03-0.95(m, 2H), 0.95-0.84 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.59; MS(ES+): 598.6 (M+1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(3,3-difluoropyrrolidine-1-carboxamido)-1H-indazole-3-carboxamide(247a)

Compound 247a was prepared from3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (235a) (300 mg, 0.29 mmol) and 3,3-difluoropyrrolidinehydrochloride (102 mg, 0.712 mmol) using TEA (0.16 mL, 1.14 mmol) asbase according to the procedure reported in step-4 of Scheme 129. Thisgave after workup, purification by flash column chromatography [silicagel (12 g), eluting with DMA80 in DCM 0 to 40%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(3,3-difluoropyrrolidine-1-carboxamido)-1H-indazole-3-carboxamide(247a) (26 mg, 0.043 mmol, 15% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.58-8.45 (m, 2H), 8.25-8.20 (m, 1H), 7.69-7.63 (m, 1H), 7.61(d, J=2.0 Hz, 1H), 7.56-7.42 (m, 2H), 7.36-7.30 (m, 1H), 7.26-7.18 (m,1H), 7.13 (td, J=7.8, 1.0 Hz, 1H), 5.62 (s, 2H), 4.33 (d, J=5.8 Hz, 2H),3.99 (s, 2H), 3.84 (t, J=13.3 Hz, 2H), 3.65 (t, J=7.4 Hz, 2H), 3.14-2.96(m, 1H), 2.49-2.38 (m, 2H), 1.06-0.96 (m, 2H), 0.93-0.83 (m, 2H); ¹⁹FNMR (282 MHz, DMSO-d₆) δ −100.42, −121.60; MS (ES+) 606.5 (M+1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(3-(pyridin-2-yl)ureido)-1H-indazole-3-carboxamide(248a)

Compound 248a was prepared from3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (235a) (286 mg, 0.27 mmol) and pyridin-2-amine (51 mg, 0.54 mmol)using TEA (0.15 mL, 1.11 mmol) as base according to the procedurereported in step-4 of Scheme 129. This gave after workup, purificationby flash column chromatography [silica gel (12 g), eluting with DMA80 inDCM 0 to 40%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(3-(pyridin-2-yl)ureido)-1H-indazole-3-carboxamide(248a) (11 mg, 0.02 mmol, 7% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 10.61 (s, 1H), 9.45 (s, 1H), 8.51 (t, J=5.9 Hz, 1H), 8.40 (d,J=2.0 Hz, 1H), 8.34-8.24 (m, 1H), 7.80-7.71 (m, 1H), 7.70-7.64 (m, 1H),7.60 (d, J=9.0 Hz, 1H), 7.55-7.42 (m, 3H), 7.36 (s, 1H), 7.27-7.19 (m,1H), 7.16-7.08 (m, 1H), 7.05-6.97 (m, 1H), 5.64 (s, 2H), 4.34 (d, J=5.7Hz, 2H), 3.99 (s, 2H), 3.13-2.97 (m, 1H), 1.05-0.97 (m, 2H), 0.96-0.83(m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.58; MS (ES+); 593.5 (M+1);(ES−): 591.5 (M−1).

Preparation ofN-(3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazol-5-yl)piperidine-1-carboxamide(249a)

Compound 249a was prepared from3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (239a) (300 mg, 0.57 mmol) and piperidine (97 mg, 1.14 mmol) usingTEA (0.32 mL, 2.28 mmol) as base according to the procedure reported instep-4 of Scheme 129. This gave after workup and purification by flashcolumn chromatography [silica gel (12 g), eluting with DMA80 in DCM 0 to40%]N-(3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazol-5-yl)piperidine-1-carboxamide(249a) (42 mg, 0.07 mmol, 13% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.63 (s, 1H), 8.48 (t, J=5.9 Hz, 1H), 8.25 (d, J=1.8 Hz, 1H),7.67-7.50 (m, 2H), 7.50-7.40 (m, 1H), 7.28-7.16 (m, 1H), 7.11 (t, J=7.8Hz, 1H), 5.69 (s, 2H), 4.35 (d, J=5.6 Hz, 2H), 4.00 (s, 2H), 3.56-3.40(m, 4H), 3.21-3.03 (m, 1H), 2.59 (s, 3H), 1.66-1.43 (m, 6H), 1.09-0.98(m, 2H), 0.97-0.80 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.61; MS(ES+): 583.6 (M+1); (ES−): 581.6 (M−1).

Preparation of tert-butyl(3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indol-6-yl)carbamate(250a)

Compound (250a) was prepared from3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indole-6-carbonylazide (219a) (210 mg, 0.4 mmol) and 2-methylpropan-2-ol (0.23 mL, 2.4mmol) using TEA (0.11 mL, 0.8 mmol) as base according to the procedurereported in step-4 of Scheme 129 to afford after workup and purificationby column chromatography [silica gel, eluting withdichloromethane/methanol (1:0 to 9:1)] tert-butyl(3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indol-6-yl)carbamate(250a) (55 mg, 24% for two steps) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 9.32 (s, 1H), 8.48 (t, J=5.8 Hz, 1H), 8.19 (s, 1H), 7.99 (d,J=8.6 Hz, 1H), 7.57 (s, 1H), 7.51-7.39 (m, 1H), 7.27-7.18 (m, 2H),7.17-7.05 (m, 1H), 5.35 (s, 2H), 4.34 (d, J=5.8 Hz, 2H), 4.00 (s, 2H),3.11-2.99 (m, 1H), 2.40 (s, 3H), 1.47 (s, 9H), 1.09-0.85 (m, 4H); ¹⁹FNMR (282 MHz, DMSO-d₆) δ −121.67; MS (ES+): 593.5 & 595.5 (M+Na).

Preparation of2-(3-acetyl-6-amino-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(251a)

Compound (251a) was prepared by hydrolysis of Boc protecting group oftert-butyl(3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indol-6-yl)carbamate(250a) (47 mg, 0.08 mmol) using 2,2,2-trifluoroacetic acid (0.127 mL,1.646 mmol) in DCM (10 mL). This gave after workup and purification byflash column chromatography [silica gel, eluting withdichloromethane/DMA 80 (1:0 to 3:1)]2-(3-acetyl-6-amino-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(251a) (26 mg, 67%) as a light brown solid; ¹H NMR (300 MHz, DMSO-d₆) δ8.48 (t, J=5.8 Hz, 1H), 7.95 (s, 1H), 7.80 (d, J=8.4 Hz, 1H), 7.47 (td,J=7.6, 1.8 Hz, 1H), 7.25 (td, J=7.3, 6.8, 1.8 Hz, 1H), 7.15 (td, J=7.9,1.0 Hz, 1H), 6.54 (dd, J=8.4, 1.9 Hz, 1H), 6.46 (d, J=1.8 Hz, 1H), 5.23(s, 2H), 4.94 (s, 2H), 4.34 (d, J=5.7 Hz, 2H), 4.00 (s, 2H), 3.10-2.97(m, 1H), 2.35 (s, 3H), 1.04-0.88 (m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.61; MS (ES+): 493.5 & 495.5 (M+Na); MS (ES−): 505.4 & 507.4 (M+Cl).

Preparation ofN-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropyl-2-(1-(methylsulfonyl)-1H-indazol-3-yl)acetamide(252a)

Compound (252a) was prepared fromN-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-2-(1H-indazol-3-yl)-N-isopropylacetamide(232b) (100 mg, 0.24 mmol) using methanesulphonic anhydride (84 mg, 0.48mmol), triethylamine (0.1 mL, 0.72 mmol), DMAP (6 mg, 0.048 mmol)according to the procedure reported in step-2 of Scheme 232.

This gave after workup and purification by flash column chromatography[silica gel (12 g), eluting with EtOAc in hexane 0 to100%]N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropyl-2-(1-(methylsulfonyl)-1H-indazol-3-yl)acetamide(252a) (21 mg, 0.042 mmol, 18% yield) as a white solid as a mixture ofrotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 8.70 and 8.48 (2t, J=5.7 Hz, 1H),7.74-7.68 and 7.68-7.61 (2m, 1H), 7.53-7.00 (m, 6H), 4.69-4.57 and4.34-4.24 (2m, 1H), 4.42 and 4.37 (2d, J=5.9 Hz, 2H), 4.12 and 4.09 (2s,2H), 3.91 and 3.81 (2s, 2H), 2.37 (s, 3H), 1.03 and 0.95 (2d, J=6.8 Hz,6H); 19F NMR (282 MHz, DMSO-d₆) δ −121.35 and −121.77; MS (ES−): 529.5(M+Cl).

Preparation of tert-butyl(3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indol-5-yl)carbamate(253a)

Compound (253a) was prepared from3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indole-5-carbonylazide (209a) (210 mg, 0.4 mmol) and 2-methylpropan-2-ol (0.23 mL, 2.4mmol) using TEA (0.11 mL, 0.8 mmol) as base according to the procedurereported in step-4 of Scheme 129 to afford after workup and purificationby column chromatography [silica gel, eluting with hexanes/10% methanolin ethyl acetate (1:0 to 1:1)] tert-butyl(3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indol-5-yl)carbamate(253a) (42 mg, 18%) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 9.22(s, 1H), 8.47 (t, J=5.9 Hz, 1H), 8.35 (d, J=1.9 Hz, 1H), 8.20 (s, 1H),7.49-7.42 (m, 1H), 7.33-7.18 (m, 3H), 7.11 (td, J=7.9, 1.0 Hz, 1H), 5.38(s, 2H), 4.35 (d, J=5.7 Hz, 2H), 3.99 (s, 2H), 3.14-2.97 (m, 1H), 2.40(s, 3H), 1.49 (s, 9H), 1.03-0.81 (m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.63; MS (ES+): 593.6 & 595.6 (M+Na); MS (ES−): 569.6 & 571.5 (M−1).

Preparation of1-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(3,3-difluoropiperidine-1-carboxamido)-1H-indazole-3-carboxamide(254d) Step-1: Preparation of methyl1-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-3-carbamoyl-1H-indazole-5-carboxylate(254a)

Reaction of 2-(3-carbamoyl-5-(methoxycarbonyl)-1H-indazol-1-yl)aceticacid (132f) TFA adduct (719 mg, 1.84 mmol) withN-(6-bromopyridin-2-yl)-2-(isopropylamino)acetamide (28b) (500 mg, 1.84mmol) according to the procedure reported in step-3 of Scheme 2 gaveafter workup and purification by flash column [silica (12 g), elutingwith DMA80 in DCM 0 to 30%] methyl1-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-3-carbamoyl-1H-indazole-5-carboxylate(254a) (865 mg, 1.63 mmol, 89% yield) as an off white solid; ¹H NMR (300MHz, DMSO-d₆) δ 11.21 and 10.82 (2s, 1H), 8.94-8.84 (m, 1H), 8.19-7.28(m, 7H), 5.70 and, 5.52 (2s, 2H), 4.67-4.54 and 4.37-4.27 (2m, 1H), 4.43and 4.03 (s, 1H), 3.90 (d, J=3.3 Hz, 3H), 1.26 (d, J=6.4 Hz) and 1.03(d, J=6.8 Hz) (2d, 6H); MS (ES⁺) 533.4 (M+2); 529.4 (M−1).

Step-2: Preparation of1-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-3-carbamoyl-1H-indazole-5-carboxylicacid (254b)

Reaction of methyl1-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-3-carbamoyl-1H-indazole-5-carboxylate(254a) (860 mg, 1.62 mmol) in MeOH/water (50 mL) with a solution oflithium hydroxide hydrate (679 mg, 16.18 mmol) in water (10 mL)according to the procedure reported in step-2 of Scheme 129 gave afterworkup1-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-3-carbamoyl-1H-indazole-5-carboxylicacid (254b) (736 g, 1.43 mmol, 88% yield) as a white solid; ¹H NMR (300MHz, DMSO-d₆) δ 12.95 (s, 1H), 11.21 and 10.82 (2s, 1H), 8.93-8.78 (m,1H), 8.26-7.16 (m, 7H), 5.67 and 5.51 (2s, 2H), 4.73-4.54 and 4.34-4.25(2m, 1H), 4.43 and 4.03 (2s, 2H), 1.25 (d, J=6.6 Hz) and 1.03 (d, J=6.7Hz) (2d, 6H); MS (ES⁻) 515.3 (M−1).

Step-3: Preparation of1-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-3-carbamoyl-1H-indazole-5-carbonylazide (254c)

Compound 254c was prepared from1-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-3-carbamoyl-1H-indazole-5-carboxylicacid (254b) (400 mg, 0.77 mmol) according to the procedure reported instep-3 of Scheme 129 to afford product (600 mg, 143% yield), which wasused in the next step without further purification.

Step-4: Preparation of1-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(3,3-difluoropiperidine-1-carboxamido)-1H-indazole-3-carboxamide(254d)

Compound (254d) was prepared from1-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-3-carbamoyl-1H-indazole-5-carbonylazide (254c) (300 mg, 0.55 mmol) and 3,3-difluoropiperidinehydrochloride (174 mg, 1.106 mmol) using TEA (0.31 mL, 2.2 mmol) as baseaccording to the procedure reported in step-4 of Scheme 129 to affordafter workup and purification by column chromatography [silica (12 g),eluting with DMA80 in DCM 0 to 40%]1-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(3,3-difluoropiperidine-1-carboxamido)-1H-indazole-3-carboxamide(254d) (32 mg, 0.05 mmol, 9% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 11.20 and 10.83 (2s, 1H), 8.78 (d, J=5.6 Hz, 1H), 8.28-7.95(m, 2H), 7.86-7.23 (m, 6H), 5.57 and 5.41 (2s, 2H), 4.71-4.52 and4.38-4.20 (m, 1H), 4.42 and 4.03 (2s, 2H), 3.81 (t, J=11.6 Hz, 2H), 3.52(bs, 2H), 2.16-1.91 (m, 2H), 1.71 (bs, 2H), 1.24 (d, J=6.3 Hz) and 1.03(d, J=6.7 Hz) (2d, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −101.17; MS (ES+):635.6 (M+1); (ES−): 633.5 (M−1).

Preparation of2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indazol-1-yl)-N-(2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)-N-cyclopropylacetamide(255b) Step-1: Preparation ofN-(2′-chloro-2-fluorobiphenyl-3-yl)-2-(cyclopropylamino)acetamide (255a)

Compound (255a) was prepared from2-chloro-N-(2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)acetamide (115b) (2g, 6.71 mmol) and cyclopropylamine (1.18 mL, 16.77 mmol) according tothe procedure reported in step-2 of scheme-115. This gave after workupand purification by flash column chromatography [silica gel 24 g,eluting with EtOAc-Hexane 10 to 100%]N-(2′-chloro-2-fluorobiphenyl-3-yl)-2-(cyclopropylamino)acetamide (255a)(1.8 g, 5.65 mmol, 84% yield) as a thick syrup; ¹H NMR (300 MHz,DMSO-d₆) δ 9.73 (s, 1H), 8.20-8.10 (m, 1H), 7.64-7.57 (m, 1H), 7.53-7.38(m, 3H), 7.26 (td, J=7.9, 1.0 Hz, 1H), 7.11-7.04 (m, 1H), 3.38 (bs, 2H),3.11 (bs, 1H), 2.24-2.12 (m, 1H), 0.43-0.34 (m, 2H), 0.32-0.23 (m, 2H);MS (ES+): 319.4 (M+1), MS (ES−): 353.3 (M+Cl).

Step-2: Preparation of2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indazol-1-yl)-N-(2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)-N-cyclopropylacetamide(255b)

Reaction ofN-(2′-chloro-2-fluorobiphenyl-3-yl)-2-(cyclopropylamino)acetamide (255a)(70 mg, 0.22 mmol) with2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indazol-1-yl)acetic acid (179b)(68 mg, 0.22 mmol) according to the procedure reported in step-3 ofscheme-2 gave after workup and purification by flash column [silica gel(12 g), eluting with DMA-80 in DCM 0-40%]2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indazol-1-yl)-N-(2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)-N-cyclopropylacetamide(255b) (90 mg, 0.15 mmol, 67% yield) as an off-white solid; ¹H NMR (300MHz, DMSO-d₆) δ 9.94 (s, 1H), 8.72 (s, 1H), 8.65 (s, 1H), 8.55 (s, 2H),7.98 (t, J=7.7 Hz, 1H), 7.90 (d, J=2.1 Hz, 1H), 7.69 (d, J=8.9 Hz, 1H),7.63-7.54 (m, 1H), 7.52-7.30 (m, 4H), 7.24 (t, J=7.9 Hz, 1H), 7.14-7.03(m, 1H), 5.77 (s, 2H), 4.24 (s, 2H), 3.22-3.10 (m, 1H), 2.60 (s, 3H),1.12-1.01 (m, 2H), 1.00-0.90 (m, 2H); 19F NMR (282 MHz, DMSO-d₆) δ−126.70; MS (ES+): 612.6 (M+1); MS (ES−): 610.6 (M−1).

Preparation of1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(3-(pyrimidin-5-yl)ureido)-1H-indazole-3-carboxamide(256a)

Compound (256a) was prepared from3-carbamoyl-1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (230b) (85 mg, 0.15 mmol) and pyrimidin-5-amine (29 mg, 0.3 mmol)according to the procedure reported in step-3 of scheme-223 to affordafter workup and purification by column chromatography [silica gel, (4g) eluting with DMA80 in DCM 0 to 50%]1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(3-(pyrimidin-5-yl)ureido)-1H-indazole-3-carboxamide(256a)

(27 mg, 0.041 mmol, 27% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) (as a mixture of two rotamers) δ 10.26 and 9.77 (2s, 1H), 9.15(s, 1H), 8.99 and 8.97 (2s, 1H), 8.94 and 8.93 (2s, 2H), 8.810 and 8.808(2s, 1H), 8.35 and 8.32 (2d, J=1.4 Hz, 1H), 8.10 and 7.95 (2t, J=7.8 Hz,1H), 7.76-7.00 (m, 10H), 5.61 and 5.47 (2s, 2H), 4.72-4.57 and 4.41-4.26(2m, 1H), 4.47 and 4.08 (2s, 2H) 1.26 and 1.06 (2d, J=6.7 Hz, 6H); 19FNMR (282 MHz, DMSO-d₆) δ −126.77 and −126.97; MS (ES−): 692.5 & 694.5(M+Cl).

Preparation of2-(3-acetyl-5-(4-fluorophenylsulfonamido)-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(257a)

To a solution of2-(3-acetyl-5-amino-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(240f) (8 mg, 0.17 mmol) in DCM (3 mL) was added Pyridine (0.069 mL,0.85 mmol), 4-fluorobenzene-1-sulfonyl chloride (49 mg, 0.25 mmol) andstirred at RT for 3h. The reaction mixture was quenched with methanol(0.5 mL), concentrated in vacuum to dryness and the residue was purifiedby flash column chromatography [silica gel (12 g), eluting with DMA80 inDCM 0 to 20%] to afford2-(3-acetyl-5-(4-fluorophenylsulfonamido)-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(257a) (70 mg, 0.11 mmol, 66% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 10.36 (s, 1H), 8.46 (t, J=5.9 Hz, 1H), 7.90-7.85 (m, 1H),7.82-7.74 (m, 2H), 7.58 (d, J=8.9 Hz, 1H), 7.52-7.31 (m, 3H), 7.27-7.16(m, 2H), 7.14-7.02 (m, 1H), 5.69 (s, 2H), 4.33 (d, J=5.7 Hz, 2H), 3.96(s, 2H), 3.15-3.01 (m, 1H), 2.56 (s, 3H), 1.07-0.95 (m, 2H), 0.94-0.82(m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −105.97, −121.58; MS (ES+): 630.5(M+1), 652.6 (M+Na); MS (ES−): 628.5 (M−1), 664.5 (M+Cl).

Preparation of2-(3-acetyl-5-(3-(pyrimidin-5-yl)ureido)-1H-indazol-1-yl)-N-(2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)-N-isopropylacetamide(258a)

Compound (256a) was prepared from3-acetyl-1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (223b) (110 mg, 0.2 mmol) and pyrimidin-5-amine (37 mg, 0.4 mmol)according to the procedure reported in step-3 of scheme-223 to affordafter workup and purification by column chromatography [silica gel, (4g) eluting with DMA80 in DCM 0 to 30%]2-(3-acetyl-5-(3-(pyrimidin-5-yl)ureido)-1H-indazol-1-yl)-N-(2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)-N-isopropylacetamide(258a) (26 mg, 0.04 mmol, 20% yield) as a white solid as a mixture ofrotamers; ¹H NMR (300 MHz, DMSO-d₆) δ 10.27 and 9.76 (2s, 1H), 9.23 (s,1H), 9.02 and 9.01 (2s, 1H), 8.94 (s, 2H), 8.82 (s, 1H), 8.41 and 8.37(2s, 1H), 8.12 and 7.96 (2t, J=8.0 Hz, 1H), 7.71-6.99 (m, 8H), 5.72 and5.55 (2s, 2H), 4.72-4.57 and 4.41-4.26 (2m, 1H), 4.47 and 4.09 (2s, 2H),2.61 and 2.60 (2s, 3H), 1.28 and 1.07 (2d, J=6.8 Hz, 6H); ¹⁹F NMR (282MHz, DMSO-d₆) δ −126.85 and −126.99; MS (ES+): 657.5 (M+1), MS (ES−):655.5 (M−1), 691.5 (M+Cl).

Preparation of1-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(piperidine-1-carboxamido)-1H-indazole-3-carboxamide(259a)

Compound (259a) was prepared from1-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-3-carbamoyl-1H-indazole-5-carbonylazide (254c) (300 mg, 0.55 mmol) and piperidine (94 mg, 1.11 mmol) usingTEA (0.31 mL, 2.2 mmol) as base according to the procedure reported instep-4 of Scheme 129 to afford after workup and purification by columnchromatography [silica (12 g), eluting with DMA80 in DCM 0 to 40%]1-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(piperidine-1-carboxamido)-1H-indazole-3-carboxamide(259a) (61 mg, 0.1 mmol, 18% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 11.20 and 10.82 (2s, 1H), 8.57 (d, J=5.1 Hz, 1H), 8.24-7.94(m, 2H), 7.86-7.27 (m, 6H), 5.56 and 5.40 (2s, 2H), 4.66-4.52 and4.35-4.26 (2m, 1H), 4.42 and 4.02 (2s, 2H), 3.52-3.38 (m, 4H), 1.62-1.46(m, 6H), 1.23 (d, J=6.4 Hz) and 1.03 (d, J=6.7 Hz) (2d, 6H); MS (ES+):599.6 (M+1); (ES−): 597.5 (M−1).

Preparation of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-N-cyclopropyl-1H-indole-5-carboxamide(260a)

Reaction of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indole-5-carboxylicacid (165b) (50 mg, 0.1 mmol) with cyclopropanamine (10.40 μL, 0.150mmol) according to the procedure reported in step-3 of Scheme 2 gaveafter workup and purification by flash column [silica (8 g), elutingdichloromethane/methanol (1:0 to 19:1)]3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-N-cyclopropyl-1H-indole-5-carboxamide(260a) (30 mg, 56%) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ8.67-8.64 (m, 1H), 8.50-8.41 (m, 2H), 8.35 (s, 1H), 7.67 (dd, J=8.7, 1.8Hz, 1H), 7.52-7.41 (m, 2H), 7.27-7.19 (m, 1H), 7.09 (td, J=7.8, 1.0 Hz,1H), 5.47 (s, 2H), 4.34 (d, J=5.7 Hz, 2H), 3.99 (s, 2H), 3.17-3.03 (m,1H), 2.96-2.79 (m, 1H), 2.45 (s, 3H), 1.05-0.82 (m, 4H), 0.75-0.55 (m,4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.59; MS (ES+): 539.5 & 541.5(M+1).

Preparation of2-(3-acetyl-5-(3-cyclopropylureido)-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(261a)

Compound (261a) was prepared from3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (217a) (105 mg, 0.2 mmol) and cyclopropanamine (0.028 mL, 0.4mmol) using TEA (0.055 mL, 0.4 mmol) as base according to the procedurereported in step-4 of Scheme 129 to afford after workup and purificationby column chromatography [silica gel (8 g), eluting withdichloromethane/methanol (1:0 to 19:1)]2-(3-acetyl-5-(3-cyclopropylureido)-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(261a) (16 mg, 14%) as an off-white solid; ¹H NMR (300 MHz, DMSO-d₆) δ8.83 (t, J=5.9 Hz) and 8.39-8.09 (m) (2H), 8.60 and 8.58 (2s, 1H),7.58-6.94 (m, 5H), 6.49-6.30 (m, 1H), 5.63 and 5.46 (2s, 2H), 4.64-4.50and 4.29-4.20 (2m, 1H), 4.46 (d, J=5.5 Hz) and 4.32 (d, J=6.0 Hz (2d,2H), 4.17 and 3.84 (2s, 2H), 2.58 and 2.41 (2s, 3H), 1.23 (d, J=6.5 Hz)and 0.99 (d, J=6.8 Hz) (2d, 6H), 0.71-0.55 (m, 2H), 0.49-0.34 (m, 2H);MS (ES−): 591.5 & 593.5 (M+Cl).

Preparation of tert-butyl(3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazol-5-yl)carbamate(262a)

Compound (262a) was prepared from3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (217a) (105 mg, 0.2 mmol) and 2-methylpropan-2-ol (0.114 mL, 1.19mmol) using TEA (0.055 mL, 0.4 mmol) as base according to the procedurereported in step-4 of Scheme 129 to afford after workup and purificationby column chromatography [silica gel, eluting withdichloromethane/methanol (1:0 to 19:1)] tert-butyl(3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazol-5-yl)carbamate(262a) (8 mg, 7%) as an off-white solid as a mixture of rotamers; ¹H NMR(300 MHz, DMSO-d₆) δ 9.47 (s, 1H), 8.83 and 8.35 (2t, 1H) 8.42 (s, 1H),7.58-6.67 (m, 5H), 5.63 and 5.46 (2s, 2H), 4.62-4.22 (m, 3H), 4.16 and3.84 (2s, 2H), 2.58 and 2.53 (2s, 3H), 1.50 and 1.49 (2s, 9H), 1.23 and0.99 (2d, J=6.8 Hz, 6H); MS (ES−): 608.6 & 610.6 (M+Cl).

Preparation of5-(3-tert-butylureido)-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(263a)

Compound 263a was prepared from3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (235a) (300 mg, 0.29 mmol) and 3,3-difluoropyrrolidinehydrochloride (102 mg, 0.712 mmol) using TEA (0.16 mL, 1.14 mmol) asbase according to the procedure reported in step-4 of Scheme 129. Thisgave after workup, purification by flash column chromatography [silicagel (12 g), eluting with DMA80 in DCM 0 to 40%]5-(3-tert-butylureido)-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(263a) (30 mg, 0.052 mmol, 14% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.46 (t, J=5.8 Hz, 1H), 8.33 (s, 1H), 8.23-8.18 (m, 1H), 7.54(s, 1H), 7.51-7.41 (m, 2H), 7.33 (dd, J=9.0, 2.0 Hz, 1H), 7.30-7.19 (m,2H), 7.17-7.07 (m, 1H), 5.88 (s, 1H), 5.59 (s, 2H), 4.33 (d, J=5.7 Hz,2H), 3.98 (s, 2H), 3.14-2.97 (m, 1H), 1.31 (s, 9H), 1.02-0.95 (m, 2H),0.95-0.85 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.59; MS (ES−) 570.4(M−1).

Preparation of (R)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-hydroxy-3-methylbutan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(264b) Step-1: Preparation of(R)—N-(3-chloro-2-fluorobenzyl)-2-((1-hydroxy-3-methylbutan-2-yl)amino)acetamide(264a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (500 mg,2.12 mmol) with (R)-2-amino-3-methylbutan-1-ol (437 mg, 4.24 mmol)according to the procedure reported in step-2 of Scheme 35 gave afterworkup(R)—N-(3-chloro-2-fluorobenzyl)-2-(1-hydroxy-3-methylbutan-2-ylamino)acetamide(264a) (641 mg, 2.12 mmol, 100% yield) which was used as such in thenext step; MS (ES+): 303.4 (M+1), 325.4 (M+Na); MS (ES−): 337.3 (M+Cl).

Step-2: Preparation of(R)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-hydroxy-3-methylbutan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(264b)

Reaction of(R)—N-(3-chloro-2-fluorobenzyl)-2-(1-hydroxy-3-methylbutan-2-ylamino)acetamide(264a) (360 mg, 1.19 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (261 mg, 1.19 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica (12 g), eluting with DMA80 in DCM 0 to 50%](R)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-hydroxy-3-methylbutan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(264b) (0.016 g, 0.032 mmol, 3% yield) as a white solid in the form ofmixture of rotamers. ¹H NMR (300 MHz, DMSO-d₆) δ 8.95 (t, J=5.7 Hz) &8.82 (t, J=5.8 Hz) (2t, 1H), 8.27-8.12 (m, 1H), 7.79 and 7.71 (2s, 1H),7.67-6.85 (m, 7H), 5.75 (bs, 1H, D₂O exchangeable), 5.70-5.39 (m, 2H),4.59-3.37 (m, 7H), 1.92-1.65 (m, 1H), 1.00 (d, J=6.4 Hz) and 0.94 (d,J=6.5 Hz) and 0.87 (d, J=6.5 Hz) and 0.76 (d, J=6.6 Hz) (4d, 6H); ¹⁹FNMR (282 MHz, DMSO-d₆) δ −121.32, −121.55; MS (ES+): 504.5 (M+1), 526.5(M+Na); MS (ES−): 502.5 (M−1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(3-(dimethylamino)piperidine-1-carboxamido)-1H-indazole-3-carboxamide(265a)

Compound 265a was prepared from3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (235a) (400 mg, 0.38 mmol) and N,N-dimethylpiperidin-3-amine (97mg, 0.76 mmol) using TEA (0.21 mL, 1.52 mmol) as base according to theprocedure reported in step-4 of Scheme 129. This gave after workup,purification by flash column chromatography [silica gel (12 g), elutingwith DMA80 in DCM 0 to 40%] followed by preparative HPLC [Cis column,eluting with CH₃CN in water (containing 0.1% TFA) 0-100%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(3-(dimethylamino)piperidine-1-carboxamido)-1H-indazole-3-carboxamide(265a) (32 mg, 0.051 mmol, 13% yield) white solid as a TFA salt; ¹H NMR(300 MHz, DMSO-d₆) δ 9.60-9.46 (m, 1H), 8.77 (s, 1H), 8.50 (t, J=5.8 Hz,1H), 8.25-8.18 (m, 1H), 7.66 (s, 1H), 7.56-7.50 (m, 2H), 7.50-7.42 (m,1H), 7.32 (s, 1H), 7.27-7.19 (m, 1H), 7.19-7.08 (m, 1H), 5.61 (s, 2H),4.33 (d, J=5.7 Hz, 2H), 4.24 (d, J=13.0 Hz, 2H), 3.98 (s, 2H), 3.94-3.88(m, 1H), 3.33-3.22 (m, 1H), 3.10-2.97 (m, 2H), 2.86 and 2.85 and 2.82and 2.81 (4s, 6H), 2.13-2.03 (m, 1H), 1.86-1.65 (m, 2H), 1.61-1.39 (m,1H), 1.03-0.95 (m, 2H), 0.95-0.85 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−73.92 (TFA peak), −121.58; MS (ES+): 627.5 (M+1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(4-(2,2-difluoroethyl)piperazine-1-carboxamido)-1H-indazole-3-carboxamide(266a)

Compound 266a was prepared from3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (235a) (400 mg, 0.38 mmol) and 1-(2,2-difluoroethyl)piperazinehydrochloride (163 mg, 0.87 mmol) using TEA (0.24 mL, 1.75 mmol) as baseaccording to the procedure reported in step-4 of Scheme 129. This gaveafter workup, purification by flash column chromatography [silica gel(12 g), eluting with DMA80 in DCM 0 to 40%] followed by preparative HPLC[C₁₈ column, eluting with CH₃CN in water (containing 0.1% TFA) 0-100%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(4-(2,2-difluoroethyl)piperazine-1-carboxamido)-1H-indazole-3-carboxamide(266a) (32 mg, 0.042 mmol, 10% yield) white solid as a TFA salt; ¹H NMR(300 MHz, DMSO-d₆) δ 8.80 (s, 1H), 8.50 (t, J=5.9 Hz, 1H), 8.21-8.15 (m,1H), 7.65 (s, 1H), 7.58-7.43 (m, 3H), 7.36-7.29 (m, 1H), 7.28-7.20 (m,1H), 7.19-7.07 (m, 2H), 5.61 (s, 2H), 4.33 (d, J=5.6 Hz, 2H), 3.98 (s,2H), 3.78-2.71 (m, 12H), 1.03-0.95 (m, 2H), 0.95-0.86 (m, 2H); ¹⁹F NMR(282 MHz, DMSO-d₆) δ −74.40 (TFA peak), −119.35, −121.59; MS (ES+) 649.5(M+1).

Preparation of5-amino-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(267e) Step-1: Preparation of ethyl2-(3-carbamoyl-5-nitro-1H-indazol-1-yl)acetate (267b)

Compound 267b was prepared from 5-nitro-1H-indazole-3-carboxamide (267a)(1.85 g, 8.97 mmol, prepared according to the procedure reported byOchs, Raymond S. and Talele; Tanaji T; in U S. Pai. Appl Publ.,20120130078) and ethyl 2-bromoacetate (1.985 mL, 17.95 mmol), usingPotassium carbonate (2.480 g, 17.95 mmol) as base according to theprocedure reported in step-1 of Scheme 56. This gave after workup ethyl2-(3-carbamoyl-5-nitro-1H-indazol-1-yl)acetate (267b) (2 g, 6.84 mmol,76% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 9.06 (dd,J=2.3, 0.7 Hz, 1H), 8.33 (dd, J=9.3, 2.3 Hz, 1H), 8.09-7.97 (m, 2H),7.73 (s, 1H), 5.60 (s, 2H), 4.18 (q, J=7.1 Hz, 2H), 1.21 (t, J=7.1 Hz,3H); MS (ES+) 293.4 (M+1), MS (ES−): 327.3 (M+Cl).

Step-2: Preparation of 2-(3-carbamoyl-5-nitro-1H-indazol-1-yl)aceticacid (267c)

Compound 267c was prepared from ethyl2-(3-carbamoyl-5-nitro-1H-indazol-1-yl)acetate (267b) (2 g, 6.84 mmol)using a solution of LiOH (0.49 g, 20.53 mmol) in Water (10 mL) as base,according to the procedure reported in step-2 of Scheme 129. This gaveafter workup 2-(3-carbamoyl-5-nitro-1H-indazol-1-yl)acetic acid (267c)(1.6 g, 6.06 mmol, 88% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 13.48 (s, 1H), 9.05 (dd, J=2.3, 0.7 Hz, 1H), 8.32 (dd, J=9.3,2.3 Hz, 1H), 8.04 (s, 1H), 8.01 (dd, J=9.3, 0.7 Hz, 1H), 7.72 (s, 1H),5.48 (s, 2H); MS (ES−): 263.2 (M−1).

Step-3: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-nitro-1H-indazole-3-carboxamide(267d)

Compound 267d was prepared from2-(3-carbamoyl-5-nitro-1H-indazol-1-yl)acetic acid (267c) (800 mg, 3.03mmol) and N-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide(10b) (933 mg, 3.63 mmol) according to the procedure reported in step-3of Scheme 2. This gave after workup and trituration with ethylacetate/hexanes (20 mL, 1:1)1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-nitro-1H-indazole-3-carboxamide(267d) (1.3 g, 2.59 mmol, 85% yield) as a off-white solid; ¹H NMR (300MHz, DMSO-d₆) δ 9.05 (dd, J=2.3, 0.6 Hz, 1H), 8.52 (t, J=5.8 Hz, 1H),8.27 (dd, J=9.3, 2.3 Hz, 1H), 8.04 (s, 1H), 7.91 (dd, J=9.3, 0.7 Hz,1H), 7.69 (s, 1H), 7.50-7.42 (m, 1H), 7.27-7.18 (m, 1H), 7.14-7.07 (m,1H), 5.78 (s, 2H), 4.33 (d, J=5.7 Hz, 2H), 3.99 (s, 2H), 3.14-3.01 (m,1H), 1.05-0.96 (m, 2H), 0.96-0.87 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.55; MS (ES+): 525.5 (M+Na), MS (ES−); 537.4 (M+Cl).

Step-4: Preparation of5-amino-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(267e)

To a solution of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-nitro-1H-indazole-3-carboxamide(267d) (1.2 g, 2.39 mmol) in THF/methanol (80 mL, 1:1) was addedammonium Chloride (2.55 g, 47.7 mmol), Zinc (1.56 g, 23.86 mmol) andstirred at RT for 3h. The mixture was filtered over a Celite pad, padwas washed with 20% methanol in EtOAc (2×10 mL) and concentratedpartially in vacuum. The resultant residue was partitioned between brine(60 mL) and EtOAc (80 mL). The organic layer was separated, dried,filtered and concentrated in vacuum. The residue obtained was purifiedby flash column chromatography [silica gel (24 g), eluting with DMA80 inDCM, 0 to 25%] to afford5-amino-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(267e) (1.05 g, 2.22 mmol, 93% yield) as light orange solid; ¹H NMR (300MHz, DMSO-d₆) δ 8.49 (t, J=5.8 Hz, 1H), 7.52-7.41 (m, 2H), 7.35-7.07 (m,5H), 6.79 (dd, J=8.9, 2.1 Hz, 1H), 5.52 (s, 2H), 5.04 (s, 2H), 4.33 (d,J=5.7 Hz, 2H), 3.97 (s, 2H), 3.09-2.98 (m, 1H), 1.02-0.93 (m, 2H),0.93-0.85 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.61; MS (ES+): 473.5(M+1), 495.4 (M+Na); MS (ES−): 507.4 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(cyclohexanecarboxamido)-1H-indazole-3-carboxamide(268a)

Compound 268a was prepared from5-amino-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(267e) (120 mg, 0.25 mmol) and cyclohexanecarboxylic acid (33 mg, 0.25mmol) according to the procedure reported in step-3 of Scheme 2. Thisgave after workup and purification by flash column chromatography[silica (12 g), eluting with DMA80 in DCM 0 to 30%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(cyclohexanecarboxamido)-1H-indazole-3-carboxamide(268a) (70 mg, 0.12 mmol, 47% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 9.91 (s, 1H), 8.50 (t, J=6.0 Hz, 1H), 8.45 (s, 1H), 7.71-7.51(m, 3H), 7.46 (td, J=7.6, 1.7 Hz, 1H), 7.35 (s, 1H), 7.28-7.18 (m, 1H),7.12 (t, J=7.9 Hz, 1H), 5.62 (s, 2H), 4.33 (d, J=5.7 Hz, 2H), 3.98 (s,2H), 3.12-2.99 (m, 1H), 2.34 (t, J=11.4 Hz, 1H), 1.91-1.11 (m, 10H),1.04-0.94 (m, 2H), 0.94-0.85 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.59; MS (ES+): 584.5 (M+1), MS (ES−): 617.5 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(2-cyclopropylacetamido)-1H-indazole-3-carboxamide(269a)

Compound 269a was prepared from5-amino-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(267e) (120 mg, 0.25 mmol) and 2-cyclopropylacetic acid (25 mg, 0.25mmol) according to the procedure reported in step-3 of Scheme 2. Thisgave after workup and purification by flash column chromatography[silica (12 g), eluting with DMA80 in DCM 0 to 30%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(2-cyclopropylacetamido)-1H-indazole-3-carboxamide(269a) (95 mg, 0.17 mmol, 68% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 9.92 (s, 1H), 8.50 (t, J=5.8 Hz, 1H), 8.44 (d, J=1.8 Hz, 1H),7.72-7.52 (m, 3H), 7.51-7.41 (m, 1H), 7.35 (s, 1H), 7.28-7.17 (m, 1H),7.12 (t, J=7.8 Hz, 1H), 5.63 (s, 2H), 4.33 (d, J=5.7 Hz, 2H), 3.98 (s,2H), 3.13-2.99 (m, 1H), 2.22 (d, J=7.0 Hz, 2H), 1.15-0.84 (m, 5H),0.55-0.43 (m, 2H), 0.26-0.16 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.59; MS (ES+): 555.5 (M+1), 577.4 (M+Na); MS (ES−): 589.4 (M+Cl).

Preparation of2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)-N-(2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)-N-cyclopropylacetamide(270a)

Compound 270a was prepared fromN-(2′-chloro-2-fluorobiphenyl-3-yl)-2-(cyclopropylamino)acetamide (255a)(80 mg, 0.25 mmol) and2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)acetic acid (97b) (78mg, 0.25 mmol) according to the procedure reported in step-3 of Scheme2. This gave after workup and purification by flash columnchromatography [silica gel (12 g), eluting with DMA-80 in DCM 0 to 40%]2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-indol-1-yl)-N-(2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)-N-cyclopropylacetamide(270a) (35 mg, 0.06 mmol, 23% yield) as an off-white solid; ¹H NMR (300MHz, DMSO-d₆) δ 9.94 (s, 1H), 8.56 (s, 1H), 8.49 (s, 1H), 8.47 (s, 2H),8.28 (s, 1H), 8.06-7.93 (m, 2H), 7.62-7.55 (m, 1H), 7.50-7.36 (m, 4H),7.24 (t, J=7.9 Hz, 1H), 7.15-7.03 (m, 2H), 5.46 (s, 2H), 4.24 (s, 2H),3.20-3.08 (m, 1H), 2.41 (s, 3H), 1.07-0.99 (m, 2H), 0.99-0.92 (m, 2H);¹⁹F NMR (282 MHz, DMSO-d₆) δ −126.77; MS (ES+): 611.6 (M+1); MS(ES−):645.5 (M+Cl).

Preparation of2-(3-acetyl-5-(pyridin-3-ylamino)-1H-indazol-1-yl)-N-(2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)-N-cyclopropylacetamide(271a)

Compound 271a was prepared fromN-(2′-chloro-2-fluorobiphenyl-3-yl)-2-(cyclopropylamino)acetamide (255a)(65 mg, 0.2 mmol) and2-(3-acetyl-5-(pyridin-3-ylamino)-1H-indazol-1-yl)acetic acid (187b) (63mg, 0.2 mmol) according to the procedure reported in step-3 of Scheme 2.This gave after workup and purification by flash column chromatography[silica gel (12 g), eluting with DMA-80 in DCM 0 to 40%]2-(3-acetyl-5-(pyridin-3-ylamino)-1H-indazol-1-yl)-N-(2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)-N-cyclopropylacetamide(271a) (40 mg, 0.07 mmol, 32% yield) as an off-white solid; ¹H NMR (300MHz, DMSO-d₆) δ 9.95 (s, 1H), 8.52 (s, 1H), 8.36 (d, J=2.7 Hz, 1H), 8.04(dd, J=4.6, 1.4 Hz, 1H), 8.02-7.94 (m, 1H), 7.87 (d, J=2.0 Hz, 1H), 7.65(d, J=9.0 Hz, 1H), 7.61-7.56 (m, 1H), 7.51-7.37 (m, 4H), 7.31-7.20 (m,3H), 7.13-7.02 (m, 1H), 5.76 (s, 2H), 4.24 (s, 2H), 3.22-3.11 (m, 1H),2.59 (s, 3H), 1.11-1.00 (m, 2H), 1.00-0.88 (m, 2H); ¹⁹F NMR (282 MHz,DMSO-d₆) δ −126.71; MS (ES+): 611.6 (M+1), MS (ES−): 645.5 (M+Cl).

Preparation ofN6-benzyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3,6-dicarboxamide(272a)

Compound 272a was prepared from3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-6-carboxylicacid (208a) (50 mg, 0.1 mmol) and phenylmethanamine (0.016 mL, 0.15mmol) according to the procedure reported in step-3 of Scheme 2. Thisgave after workup and purification by flash column chromatography[silica gel (8 g), eluting with dichloromethane/methanol (1:0 to 19:1)]N6-benzyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3,6-dicarboxamide(272a) (36 mg, 61% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ9.14 (t, J=6.0 Hz, 1H), 8.55 (t, J=5.8 Hz, 1H), 8.26-8.19 (m, 2H), 7.83(s, 1H), 7.79 (dd, J=8.5, 1.4 Hz, 1H), 7.51-7.16 (m, 8H), 7.08 (td,J=7.9, 1.0 Hz, 1H), 5.74 (s, 2H), 4.52 (d, J=5.9 Hz, 2H), 4.30 (d, J=5.7Hz, 2H), 4.00 (s, 2H), 3.19-2.98 (m, 1H), 1.06-0.87 (m, 4H); ¹⁹F NMR(282 MHz, DMSO-d₆) δ −121.57; MS (ES−): 625.5 & 627.6 (M+Cl).

Preparation of tert-butyl(3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazol-6-yl)carbamate(273a)

Compound 273a was prepared from3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-6-carbonylazide (236a) (210 mg, 0.4 mmol) and 2-methylpropan-2-ol (0.23 mL, 2.4mmol) using TEA (0.11 mL, 0.8 mmol) as base according to the procedurereported in step-4 of Scheme 129 to afford after workup and purificationby column chromatography [silica gel, eluting with hexanes/10% methanolin ethyl acetate (1:0 to 1:1)] tert-butyl(3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazol-6-yl)carbamate(273a) (96 mg, 42%) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 9.61(s, 1H), 8.53 (t, J=5.8 Hz, 1H), 7.99 (dd, J=8.8, 0.7 Hz, 1H), 7.81 (s,1H), 7.68 (s, 1H), 7.45 (td, J=7.5, 1.7 Hz, 1H), 7.34 (s, 1H), 7.27-7.07(m, 3H), 5.58 (s, 2H), 4.33 (d, J=5.7 Hz, 2H), 3.99 (s, 2H), 3.16-2.99(m, 1H), 1.49 (s, 9H), 1.07-0.83 (m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.65; MS (ES+): 595.5 & 597.5 (M+Na); MS (ES−): 607.4 & 609.4 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(4-(2-methoxyethyl)piperazine-1-carboxamido)-1H-indazole-3-carboxamide(274a)

Compound 274a was prepared from3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (235a) (460 mg, 0.44 mmol) and 1-(2-methoxyethyl)piperazine (126mg, 0.87 mmol) using TEA (0.24 mL, 1.75 mmol) as base according to theprocedure reported in step-4 of Scheme 129. This gave after workup,purification by flash column chromatography [silica gel (12 g), elutingwith DMA80 in DCM 0 to 40%] followed by preparative HPLC [C₁₈ column,eluting with CH₃CN in water (containing 0.1% TFA) 0-100%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(4-(2-methoxyethyl)piperazine-1-carboxamido)-1H-indazole-3-carboxamide(274a) (25 mg, 0.04 mmol, 9% yield) white solid as a TFA salt; ¹H NMR(300 MHz, DMSO-d₆) δ 8.64 (s, 1H), 8.50 (t, J=5.8 Hz, 1H), 8.23-8.12 (m,1H), 7.63 (s, 1H), 7.58-7.41 (m, 3H), 7.32 (s, 1H), 7.27-7.19 (m, 1H),7.18-7.07 (m, 1H), 5.61 (s, 2H), 4.33 (d, J=5.7 Hz, 2H), 3.98 (s, 2H),3.49-3.42 (m, 5H), 3.35 (s, 3H), 3.24 (s, 3H), 3.14-2.97 (m, 1H),2.47-2.38 (m, 4H), 1.04-0.94 (m, 2H), 0.94-0.81 (m, 2H); ¹⁹F NMR (282MHz, DMSO) δ −73.44 (TFA peak), −121.60; MS (ES+): 643.6 (M+1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(3-(2-(dimethylamino)ethyl)-3-methylureido)-1H-indazole-3-carboxamide(275a)

Compound 275a was prepared from3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (235a) (500 mg, 0.47 mmol) andN1,N1,N2-trimethylethane-1,2-diamine (97 mg, 0.95 mmol) using TEA (0.27mL, 1.9 mmol) as base according to the procedure reported in step-4 ofScheme 129. This gave after workup, purification by flash columnchromatography [silica gel (12 g), eluting with DMA80 in DCM 0 to 40%]followed by preparative HPLC [C₁₈ column, eluting with CH₃CN in water(containing 0.1% TFA) 0-100%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(3-(2-(dimethylamino)ethyl)-3-methylureido)-1H-indazole-3-carboxamide(275a) (22 mg, 0.04 mmol, 8% yield) white solid as a TFA salt; ¹H NMR(300 MHz, DMSO-d₆) δ 8.93 (s, 1H), 8.50 (t, J=5.8 Hz, 1H), 8.21-8.13 (m,1H), 7.61 (bs, 1H), 7.53-7.41 (m, 3H), 7.30 (s, 1H), 7.26-7.18 (m, 1H),7.18-7.08 (m, 1H), 5.61 (s, 2H), 4.33 (d, J=5.7 Hz, 2H), 3.98 (s, 2H),3.41 (t, J=6.3 Hz, 2H), 3.12-3.01 (m, 1H), 2.96 (s, 3H), 2.47-2.41 (m,2H), 2.23 (s, 6H), 1.03-0.95 (m, 2H), 0.95-0.87 (m, 2H); ¹⁹F NMR (282MHz, DMSO) δ −73.44 (TFA peak), −121.61; MS (ES+): 601.6 (M+1); MS(ES−): 599.5 (M−1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-((pyridin-3-ylmethyl)amino)-1H-indazole-3-carboxamide(276a)

To a solution of5-amino-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(267e) (100 mg, 0.21 mmol) in DMF (2 mL) and acetic acid (1 mL) wasadded nicotinaldehyde (230 mg, 0.21 mmol) and stirred at RT for 1h. Tothe red colored solution was added in portion wise sodiumcyanoborohydride (130 mg, 0.21 mmol) and continued stirring at RT for 16h. The reaction mixture was diluted with saturated aqueous NaHCO₃solution (50 mL) and extracted with EtOAc (2×50 mL). The organic layerswere combined washed with brine, dried, filtered and concentrated invacuum. The residue obtained was purified by flash column chromatography[silica gel (24 g), eluting with DMA80 in DCM 0 to 40%] to afford1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-((pyridin-3-ylmethyl)amino)-1H-indazole-3-carboxamide(276a) (40 mg, 0.07 mmol, 34% yield) as white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.64 (d, 1H), 8.54-8.43 (m, 2H), 7.90-7.81 (m, 1H), 7.51-7.33(m, 5H), 7.27-7.06 (m, 4H), 6.93 (dd, J=9.1, 2.2 Hz, 1H), 5.53 (s, 2H),4.39-4.28 (m, 4H), 3.97 (s, 2H), 3.10-2.98 (m, 1H), 1.01-0.93 (m, 2H),0.93-0.84 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.60; MS (ES+): 564.5(M+1), 586.5 (M+Na), MS (ES−): 598.4, 600.4 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(3,3-dimethylureido)-1H-indazole-3-carboxamide(277a)

Compound 277a was prepared from3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (235a) (500 mg, 0.47 mmol) and dimethylamine (2M in THF) (0.47 mL,0.95 mmol) using TEA (0.27 mL, 1.9 mmol) as base according to theprocedure reported in step-4 of Scheme 129. This gave after workup,purification by flash column chromatography [silica gel (12 g), elutingwith DMA80 in DCM 0 to 40%] followed by preparative HPLC [C₁₈ column,eluting with CH₃CN in water (containing 0.1% TFA) 0-100%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(3,3-dimethylureido)-1H-indazole-3-carboxamide(277a) (26 mg, 0.048 mmol, 11% yield) white solid as a TFA salt; ¹H NMR(300 MHz, DMSO-d₆) δ 8.51 (t, J=5.8 Hz, 1H), 8.43 (s, 1H), 8.21-8.15 (m,1H), 7.63 (s, 1H), 7.60-7.53 (m, 1H), 7.52-7.42 (m, 2H), 7.31 (s, 1H),7.27-7.19 (m, 1H), 7.18-7.09 (m, 1H), 5.61 (s, 2H), 4.33 (d, J=5.7 Hz,2H), 3.98 (s, 2H), 3.10-3.00 (m, 1H), 2.94 (s, 6H), 1.04-0.95 (m, 2H),0.95-0.85 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −73.47 (TFA peak),−121.61; MS (ES+) 544.5 (M+1); (ES−) 542.5 (M−1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(4-(4-fluorobenzyl)piperazine-1-carboxamido)-1H-indazole-3-carboxamide(278a)

Compound 278a was prepared from3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (235a) (750 mg, 0.71 mmol) and 1-(4-fluorobenzyl)piperazine (276mg, 1.423 mmol) using TEA (0.4 mL, 2.85 mmol) as base according to theprocedure reported in step-4 of Scheme 129. This gave after workup,purification by flash column chromatography [silica gel (12 g), elutingwith DMA80 in DCM 0 to 40%] followed by preparative HPLC [C₁₈ column,eluting with CH₃CN in water (containing 0.1% TFA) 0-100%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(4-(4-fluorobenzyl)piperazine-1-carboxamido)-1H-indazole-3-carboxamide(278a) (35 mg, 6% yield) white solid as a TFA salt; ¹H NMR (300 MHz,DMSO-d₆) δ 10.13 (s, 1H), 8.92 (s, 1H), 8.52 (t, J=5.9 Hz, 1H),8.25-8.12 (m, 1H), 7.67 (s, 1H), 7.62-7.51 (m, 4H), 7.46 (td, J=7.6, 1.8Hz, 1H), 7.40-7.30 (m, 3H), 7.28-7.18 (m, 1H), 7.18-7.08 (m, 1H), 5.62(s, 2H), 4.38 (s, 2H), 4.36-4.17 (m, 4H), 3.98 (s, 2H), 3.45-2.98 (m,7H), 1.07-0.96 (m, 2H), 0.96-0.85 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−74.05 (TFA peak), −111.72, −121.59; MS (ES+) 693.6 (M+1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(3-methyl-3-(1-methylpiperidin-4-yl)ureido)-1H-indazole-3-carboxamide(279a)

Compound 279a was prepared from3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (235a) (500 mg, 0.47 mmol) and N,1-dimethylpiperidin-4-amine (122mg, 0.95 mmol), using TEA (0.13 mL, 0.95 mmol) as base according to theprocedure reported in step-4 of Scheme 129. This gave after workup,purification by flash column chromatography [silica gel (12 g), elutingwith DMA80 in DCM 0 to 40%] followed by preparative HPLC [C₁₈ column,eluting with CH₃CN in water (containing 0.1% TFA) 0-100%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(3-methyl-3-(1-methylpiperidin-4-yl)ureido)-1H-indazole-3-carboxamide(279a) (68 mg, 19% yield) white solid as a TFA salt; ¹H NMR (300 MHz,DMSO-d₆) δ 9.51 (s, 1H), 8.55-8.44 (m, 2H), 8.22-8.16 (m, 1H), 7.65 (s,1H), 7.57-7.51 (m, 2H), 7.51-7.41 (m, 1H), 7.35-7.27 (m, 1H), 7.27-7.19(m, 1H), 7.18-7.09 (m, 1H), 5.61 (s, 2H), 4.36-4.29 (m, 3H), 3.98 (s,2H), 3.56-3.40 (m, 2H), 3.16-2.98 (m, 3H), 2.84 (s, 3H), 2.79 and 2.78(2s, 3H), 2.04-1.86 (m, 2H), 1.86-1.74 (m, 2H), 1.02-0.94 (m, 2H),0.94-0.85 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −73.93 (TFA peak),−121.60; MS (ES+): 627.6 (M+1).

Preparation of2-(3-acetyl-5-(pyrimidin-5-yl)-1H-indazol-1-yl)-N-(2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)-N-isopropylacetamide(280b) Step-1: Preparation of2-(3-acetyl-5-bromo-1H-indazol-1-yl)-N-(2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)-N-isopropylacetamide(280a)

Compound 280a was prepared fromN-(2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-2-(isopropylamino)acetamide(115c) (190 mg, 0.59 mmol) and2-(3-acetyl-5-bromo-1H-indazol-1-yl)acetic acid (156e) (160 mg, 0.54mmol) according to the procedure reported in step-3 of Scheme 2. Thisgave after workup and purification by flash column chromatography[silica (12 g), eluting with DMA80 in DCM from 0 to 30%]2-(3-acetyl-5-bromo-1H-indazol-1-yl)-N-(2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)-N-isopropylacetamide(280a) (280 mg, 0.47 mmol, 87% yield) as an off white solid; ¹H NMR (300MHz, DMSO-d₆) δ 10.26 and 9.74 (2s, 1H), 8.11 and 7.94 (2t, J=7.8 Hz,1H), 7.72-7.54 (m, 4H), 7.54-7.36 (m, 3H), 7.36-7.01 (m, 2H), 5.78 and5.60 (2s, 2H), 4.70-4.55 and 4.38-4.23 (2m, 1H), 4.46 and 4.08 (2s, 2H),2.62 and 2.61 (2s, 3H), 1.28 and 1.07 (2d, J=6.8 Hz, 6H); MS (ES−):635.3, 637.3 (M+Cl).

Step-2: Preparation of2-(3-acetyl-5-(pyrimidin-5-yl)-1H-indazol-1-yl)-N-(2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)-N-isopropylacetamide(280b)

Compound 280b was prepared from2-(3-acetyl-5-bromo-1H-indazol-1-yl)-N-(2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)-N-isopropylacetamide(280a) (120 mg, 0.20 mmol), and pyrimidin-5-ylboronic acid (0.025 g,0.200 mmol) according to the procedure reported in Scheme 100. This gaveafter workup and purification by flash column chromatography [silica (12g), eluting with DMA80 in DCM from 0 to 30%]2-(3-acetyl-5-(pyrimidin-5-yl)-1H-indazol-1-yl)-N-(2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)-N-isopropylacetamide(280b) (55 mg, 0.09 mmol, 46% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 10.28 and 9.75 (2s, 1H), 9.23 and 9.22 (2s, 1H), 9.19 and9.17 (2s, 2H), 8.50-8.48 and 8.50-8.43 (2m, 1H), 8.18-7.80 (m, 3H),7.67-7.00 (m, 6H), 5.83 and 5.64 (2s, 2H), 4.72-4.58 and 4.41-4.28 (2m,1H), 4.49 and 4.10 (2s, 2H), 2.66 and 2.65 (2s, 3H), 1.30 and 1.08 (2d,J=6.8 Hz, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −126.91; MS (ES−): 597.4(M−1), 633.5 (M+Cl).

Preparation of2-(3-acetyl-5-(2-oxopyrrolidin-1-yl)-1H-indol-1-yl)-N-(2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)-N-cyclopropylacetamide(281c) Step-1: Preparation of tert-butyl2-(3-acetyl-5-(2-oxopyrrolidin-1-yl)-1H-indol-1-yl)acetate (281a)

Compound 281a was prepared from tert-butyl2-(3-acetyl-5-bromo-1H-indol-1-yl)acetate (90b) (500 mg, 1.42 mmol) andpyrrolidin-2-one (121 mg, 1.42 mmol), according to the procedurereported in Scheme 92. This gave after workup and purification by flashcolumn chromatography [silica (24 g), eluting with methanol in DCM from0 to 100%] tert-butyl2-(3-acetyl-5-(2-oxopyrrolidin-1-yl)-1H-indol-1-yl)acetate (281a) (256mg, 0.72 mmol, 51% yield) as a brown wax; MS (ES+): 357.4 (M+1), 379.4(M+Na); MS (ES−): 391.3 (M+Cl).

Step-2: Preparation of2-(3-acetyl-5-(2-oxopyrrolidin-1-yl)-1H-indol-1-yl)acetic acid (281b)

Compound 281b was prepared from tert-butyl2-(3-acetyl-5-(2-oxopyrrolidin-1-yl)-1H-indol-1-yl)acetate (281a) (256mg, 0.72 mmol) using TFA (1.66 mL, 21.55 mmol), according to theprocedure reported in step-2 of Scheme 2. This gave after workup2-(3-acetyl-5-(2-oxopyrrolidin-1-yl)-1H-indol-1-yl)acetic acid (281b)(298 mg, 0.72 mmol, 100% yield) yellow solid as a TFA salt; MS (ES+):323.4 (M+Na); MS (ES−): 299.3 (M−1).

Step-3: Preparation of2-(3-acetyl-5-(2-oxopyrrolidin-1-yl)-1H-indol-1-yl)-N-(2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)-N-cyclopropylacetamide(281c)

Compound 281c was prepared from2-(3-acetyl-5-(2-oxopyrrolidin-1-yl)-1H-indol-1-yl)acetic acid (281b)(150 mg, 0.36 mmol) andN-(2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-2-(cyclopropylamino)acetamide(255a) (138 mg, 0.43 mmol) according to the procedure reported in step-3of Scheme 2. This gave after workup and purification by flash columnchromatography [First Column: silica gel (24 g), eluting with methanolin DCM 0-20%; second column: Silica gel (24 g), eluting with ethylacetate/methanol (9:1) in hexanes 0-100%]]2-(3-acetyl-5-(2-oxopyrrolidin-1-yl)-1H-indol-1-yl)-N-(2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)-N-cyclopropylacetamide(281c) (25 mg, 0.042 mmol, 12% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 9.94 (s, 1H), 8.31 (s, 1H), 8.28-8.22 (m, 1H), 8.03-7.96 (m,1H), 7.65-7.53 (m, 2H), 7.52-7.36 (m, 4H), 7.25 (t, J=7.9 Hz, 1H),7.12-7.05 (m, 1H), 5.48 (s, 2H), 4.24 (s, 2H), 3.87 (t, J=7.0 Hz, 2H),3.20-3.07 (m, 1H), 2.52-2.43 (m, 2H), 2.42 (s, 3H), 2.17-2.01 (m, 2H),1.07-0.91 (m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −126.79; MS (ES+): 601.5(M+1), 623.5 (M+Na); MS (ES−): 599.5 (M−1).

Preparation of1-(2-(cyclopropyl(2-((2-fluoro-2′-methyl-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(282e) Step-1: Preparation ofN-(3-bromo-2-fluorophenyl)-2-chloroacetamide (282b)

To a biphasic solution of 3-bromo-2-fluoroaniline (282a) (5 g, 26.3mmol) in EtOAc (100 mL), saturated aqueous NaHCO₃ (100 mL) was addedchloroacetyl chloride (35a) (2.11 mL, 26.3 mmol) and stirred at RT for2h. The organic layer was separated washed with brine, dried, filteredand concentrated in vacuum to affordN-(3-bromo-2-fluorophenyl)-2-chloroacetamide (282b) (7 g, 26.3 mmol,100% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 10.27 (s, 1H),7.85 (ddd, J=8.5, 7.2, 1.6 Hz, 1H), 7.50 (ddd, J=8.1, 6.4, 1.6 Hz, 1H),7.16 (td, J=8.1, 1.4 Hz, 1H), 4.37 (s, 2H); MS (ES−): 264.1, 266.1(M−1).

Step-2: Preparation ofN-(3-bromo-2-fluorophenyl)-2-(cyclopropylamino)acetamide (282c)

Compound 282c was prepared fromN-(3-bromo-2-fluorophenyl)-2-chloroacetamide (282b) (5.0 g, 18.76 mmol)and cyclopropylamine (3.31 mL, 46.9 mmol) according to the procedurereported in step-1 of Scheme 35. This gave after workupN-(3-bromo-2-fluorophenyl)-2-(cyclopropylamino)acetamide (282c) (5.3 g,18.46 mmol, 98% yield) as a thick syrup which was used as such withoutany purification; ¹H NMR (300 MHz, DMSO-d₆) δ 9.87 (bs, 1H), 7.99 (ddd,J=8.2, 7.2, 1.6 Hz, 1H), 7.43 (ddd, J=8.1, 6.5, 1.6 Hz, 1H), 7.14 (td,J=8.2, 1.5 Hz, 1H), 3.35 (s, 2H), 2.18 (m, 1H), 0.43-0.35 (m, 2H),0.35-0.26 (m, 2H).

Step-3: Preparation of1-(2-((2-((3-bromo-2-fluorophenyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(282d)

Compound 282d was prepared from 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (2.52 g, 11.5 mmol) andN-(3-bromo-2-fluorophenyl)-2-(cyclopropylamino)acetamide (282c) (3 g,10.45 mmol) according to the procedure reported in step-3 of Scheme 2.This gave after workup1-(2-((2-((3-bromo-2-fluorophenyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(282d) (4 g, 79% yield) as a white solid which was used as such withoutfurther purification; ¹H NMR (300 MHz, DMSO-d₆) δ 10.02 (s, 1H), 8.18(dt, J=8.2, 1.0 Hz, 1H), 7.89-7.80 (m, 1H), 7.72 (s, 1H), 7.66 (dt,J=8.6, 0.9 Hz, 1H), 7.49-7.35 (m, 3H), 7.30-7.22 (m, 1H), 7.12 (td,J=8.2, 1.4 Hz, 1H), 5.70 (s, 2H), 4.22 (s, 2H), 3.18-3.05 (m, 1H),1.08-0.99 (m, 2H), 0.99-0.92 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−118.11; MS (ES+) 488.4, 490.4 (M+1), 510.3, 512.3 (M+Na), MS (ES−):522.3, 524.3 (M+Cl).

Step-4: Preparation of1-(2-(cyclopropyl(2-((2-fluoro-2′-methyl-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(282e)

Compound 282e was prepared from1-(2-((2-((3-bromo-2-fluorophenyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(282d) (150 mg, 0.31 mmol), and o-tolylboronic acid (50 mg, 0.37 mmol)according to the procedure reported in Scheme 100. This gave afterworkup and purification by flash column chromatography [silica (12g),eluting with DMA80 in DCM from 0 to 20%]1-(2-(cyclopropyl(2-((2-fluoro-2′-methyl-[1,1′-biphenyl]-3-yl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(282e) (85 mg, 0.17 mmol, 55% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 9.91 (s, 1H), 8.18 (dt, J=8.1, 1.1 Hz, 1H), 7.91 (t, J=7.3Hz, 1H), 7.74 (bs, 1H), 7.67 (dt, J=8.6, 1.0 Hz, 1H), 7.48-7.36 (m, 2H),7.35-7.15 (m, 6H), 7.06-6.99 (m, 1H), 5.71 (s, 2H), 4.23 (s, 2H),3.19-3.07 (m, 1H), 2.12 (s, 3H), 1.03 (s, 2H), 1.00-0.91 (m, 2H); 19FNMR (282 MHz, DMSO-d₆) δ −127.47; MS (ES+) 500.5 (M+1), MS (ES−): 498.5(M−1), 534.4 (M+Cl).

Preparation of1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(283a)

Compound 283a was prepared from1-(2-((2-((3-bromo-2-fluorophenyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(282d) (150 mg, 0.31 mmol), and 2-chlorophenylboronic acid (62 mg, 0.38mmol) according to the procedure reported in Scheme 100. This gave afterworkup and purification by flash column chromatography [silica gel (12g), eluting with DMA80 in DCM 0 to 20%]1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(283a) (95 mg, 0.18 mmol, 60% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 9.95 (s, 1H), 8.18 (dt, J=8.1, 1.0 Hz, 1H), 8.04-7.91 (m,1H), 7.74 (s, 1H), 7.70-7.63 (m, 1H), 7.62-7.55 (m, 1H), 7.52-7.34 (m,5H), 7.30-7.19 (m, 2H), 7.12-7.03 (m, 1H), 5.71 (s, 2H), 4.23 (s, 2H),3.19-3.06 (m, 1H), 1.07-1.00 (m, 2H), 1.00-0.92 (m, 2H); ¹⁹F NMR (282MHz, DMSO-d₆) δ −126.75; MS (ES+): 520.4 (M+1), 542.4 (M+Na); MS (ES−):518.4 (M−1).

Preparation ofN-(3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazol-4-yl)-3,3-difluoropiperidine-1-carboxamide(284i) Step-1: Preparation of methyl 3-iodo-1H-indazole-4-carboxylate(284b)

Compound 284b was prepared from methyl 1H-indazole-4-carboxylate (284a)(5 g, 28.4 mmol) according to the procedure reported in step-1 of Scheme132. This gave after work up and purification by flash chromatography[silica gel, (40 g) eluting with EtOAc in hexane 0-60%] methyl3-iodo-1H-indazole-4-carboxylate (284b) (6.6 g, 21.85 mmol, 77% yield)as an off white solid. ¹H NMR (300 MHz, DMSO-d₆) δ 13.89 (s, 1H),7.87-7.74 (m, 1H), 7.53-7.44 (m, 2H), 4.00 (s, 3H); MS (ES+) 303.2(M+1); (ES−) 301.2 (M−1).

Step-2: Preparation methyl1-(2-(tert-butoxy)-2-oxoethyl)-3-iodo-1H-indazole-4-carboxylate (284c)

Compound 284c was prepared from methyl 3-iodo-1H-indazole-4-carboxylate(132b) (6.6 g, 21.85 mmol) and tert-butyl 2-bromoacetate (6.39 g, 32.8mmol) according to the procedure reported in step-1 of Scheme 56. Thisgave after workup and trituration of solid with methanol (5 mL) methyl1-(2-tert-butoxy-2-oxoethyl)-3-iodo-1H-indazole-4-carboxylate (284c)(6.6 g, 15.86 mmol, 73% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 7.92 (dd, J=7.9, 1.5 Hz, 1H), 7.64-7.43 (m, 2H), 5.38 (s,2H), 3.95 (s, 3H), 1.41 (s, 9H); MS (ES+) 417.4 (M+1), 439.3 (M+Na).

Step-3: Preparation of methyl3-acetyl-1-(2-(tert-butoxy)-2-oxoethyl)-1H-indazole-4-carboxylate (284d)

Compound 284d was prepared from methyl1-(2-(tert-butoxy)-2-oxoethyl)-3-iodo-1H-indazole-4-carboxylate (284c)(2.05 g, 4.91 mmol) according to the procedure reported in step-1 andstep-2 of Scheme 206. This gave after work up and purification by flashchromatography [silica gel, (40 g) eluting with EtOAc in hexane 0-50%]methyl 3-acetyl-1-(2-(tert-butoxy)-2-oxoethyl)-1H-indazole-4-carboxylate(284d) (1.44 g, 4.33 mmol, 88% yield) as a yellow solid; ¹H NMR (300MHz, DMSO-d₆) δ 7.94 (dd, J=8.4, 0.9 Hz, 1H), 7.62-7.54 (m, 1H), 7.49(dd, J=7.1, 0.9 Hz, 1H), 5.50 (s, 2H), 3.83 (s, 3H), 2.62 (s, 3H), 1.42(s, 9H); MS (ES+) 333.3 (M+1); 355.3 (M+Na); (ES−) 331.3 (M−1).

Step-4: Preparation of2-(3-acetyl-4-(methoxycarbonyl)-1H-indazol-1-yl)acetic acid (284e)

Compound 284e was prepared from methyl3-acetyl-1-(2-(tert-butoxy)-2-oxoethyl)-1H-indazole-4-carboxylate (284d)(1.44 g, 4.33 mmol) and TFA (2.0 mL, 26.0 mmol), according to theprocedure reported in step-2 of Scheme 2. This gave after work up2-(3-acetyl-4-(methoxycarbonyl)-1H-indazol-1-yl)acetic acid (284e) (1.11g, 4.02 mmol, 93% yield) as a brown solid, which was used as such in thenext step without further purification. MS (ES+) 277.3 (M+1).

Step-5: Preparation of methyl3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-4-carboxylate(284f)

Compound 284f was prepared from2-(3-acetyl-4-(methoxycarbonyl)-1H-indazol-1-yl)acetic acid (284e) (788mg, 2.85 mmol) andN-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide (10b) (769 mg,3.00 mmol) according to the procedure reported in step-3 of Scheme 2.This gave after workup and purification by flash column [silica (12g),eluting with DMA80 in DCM 0 to 30%] methyl3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-4-carboxylate(284f) (950 mg, 1.85 mmol, 65% yield) as a yellow solid. MS (ES⁻) 513.5(M−1).

Step-6: Preparation of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-4-carboxylicacid (284g)

Compound 284g was prepared from methyl3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-4-carboxylate(284f) (850 mg, 1.651 mmol) and lithium hydroxide monohydride (416 mg,9.90 mmol) in water (10 mL) according to the procedure reported instep-2 of Scheme 129. This gave after work up3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-4-carboxylicacid (284g) (827 mg, 1.65 mmol, 100% yield) as a white solid, which wasused as such in the next step without further purification. ¹H NMR (300MHz, DMSO-d₆) δ 8.48 (t, J=5.8 Hz, 1H), 7.86-7.78 (m, 1H), 7.53-7.41 (m,3H), 7.27-7.18 (m, 1H), 7.10 (td, J=7.8, 1.0 Hz, 1H), 5.78 (s, 2H), 4.34(d, J=5.7 Hz, 2H), 3.99 (s, 2H), 3.19-3.03 (m, 1H), 2.60 (s, 3H),1.12-0.99 (m, 2H), 0.98-0.83 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−74.96 (TFA peak), −121.61; MS (ES+): 501.4 (M+1), (ES−): 499.3 (M−1).

Step-7: Preparation of3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-4-carbonylazide (284h)

Compound 284h was prepared from3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-4-carboxylicacid (284g) (320 mg, 0.639 mmol) according to the procedure reported instep-3 of Scheme 129. This gave after work up3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-4-carbonylazide (284h) (300 mg, 0.57 mmol, 89% yield) which was used as such inthe next step without further purification; MS (ES−): 560.3 (M+Cl).

Step-8: Preparation ofN-(3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazol-4-yl)-3,3-difluoropiperidine-1-carboxamide(284i)

Compound 284i was prepared from3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-4-carbonylazide (284h) (150 mg, 0.285 mmol) and 3,3-difluoropiperidinehydrochloride (90 mg, 0.57 mmol) using TEA (0.16 mL, 1.14 mmol) as baseaccording to the procedure reported in step-4 of Scheme 129 to affordafter workup and purification by column chromatography [First column:silica gel (12g), eluting with DMA80 in DCM 0 to 40%, second column:silica gel (12g), eluting with ethyl acetate/methanol (9:1) in hexanes 0to 100%]N-(3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazol-4-yl)-3,3-difluoropiperidine-1-carboxamide(284i) (20 mg, 0.032 mmol, 11.33% yield) as a white solid; ¹H NMR (300MHz, DMSO-d₆) δ 10.84 (s, 1H), 8.48 (t, J=5.8 Hz, 1H), 8.14-8.02 (m,1H), 7.50-7.43 (m, 1H), 7.37 (t, J=8.1 Hz, 1H), 7.28-7.17 (m, 2H),7.15-7.05 (m, 1H), 5.74 (s, 2H), 4.34 (d, J=5.7 Hz, 2H), 3.99 (s, 2H),3.91 (t, J=12.0 Hz, 2H), 3.72-3.56 (m, 2H), 3.19-3.07 (m, 1H), 2.74 (s,3H), 2.20-2.02 (m, 2H), 1.86-1.75 (m, 2H), 1.09-0.96 (m, 2H), 0.96-0.82(m, 2H); ¹⁹F NMR (282 MHz, DMSO) δ −101.19; −121.60; MS (ES+): 641.5(M+Na); (ES−): 617.4 (M−1).

Preparation ofN-(3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazol-4-yl)-3,3-difluoroazetidine-1-carboxamide(285a)

Compound 285a was prepared from3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-4-carbonylazide (284h) (150 mg, 0.285 mmol) and 3,3-difluoroazetidinehydrochloride (73.9 mg, 0.570 mmol) using TEA (0.16 mL, 1.14 mmol) asbase according to the procedure reported in step-4 of Scheme 129 toafford after workup and purification twice by column chromatography[silica gel (12 g), eluting with DMA80 in DCM 0 to 40%]N-(3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazol-4-yl)-3,3-difluoroazetidine-1-carboxamide(285a) (25 mg, 0.042 mmol, 15% yield) as a yellow solid; ¹H NMR (300MHz, DMSO-d₆) δ 10.92 (s, 1H), 8.48 (t, J=5.8 Hz, 1H), 8.11 (d, J=7.7Hz, 1H), 7.52-7.43 (m, 1H), 7.43-7.33 (m, 1H), 7.31-7.18 (m, 2H),7.16-7.03 (m, 1H), 5.73 (s, 2H), 4.54 (t, J=12.6 Hz, 4H), 4.34 (d, J=5.7Hz, 2H), 3.99 (s, 2H), 3.19-3.06 (m, 1H), 2.73 (s, 3H), 1.09-0.97 (m,2H), 0.97-0.84 (m, 2H); ¹⁹F NMR (282 MHz, DMSO) δ −99.58; −121.59; MS(ES+): 591.5 (M+1); MS (ES−): 589.4 (M−1); 625.5 (M+Cl).

Preparation of2-(3-acetyl-5-amino-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(286a)

Compound 286a was prepared from tert-butyl(3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indol-5-yl)carbamate(253a) (20 mg, 0.035 mmol) and 2,2,2-trifluoroacetic acid (0.16 mL, 2.1mmol) according to the procedure reported in step-2 of Scheme 2. Thisgave after workup and purification by flash column chromatography[silica gel (4 g), eluting with dichloromethane/DMA 80 (1:0 to 3:1)]2-(3-acetyl-5-amino-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(286a) (12 mg, 73%) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 8.46(t, J=5.9 Hz, 1H), 8.03 (s, 1H), 7.50-7.43 (m, 1H), 7.40 (d, J=2.1 Hz,1H), 7.27-7.20 (m, 1H), 7.16-7.07 (m, 2H), 6.54 (dd, J=8.7, 2.2 Hz, 1H),5.29 (s, 2H), 4.81 (s, 2H), 4.34 (d, J=5.7 Hz, 2H), 3.98 (s, 2H),3.15-2.96 (m, 1H), 2.35 (s, 3H), 1.04-0.79 (m, 4H); ¹⁹F NMR (282 MHz,DMSO-d₆) δ −121.63; MS (ES+): 471.4 (M+1); MS (ES−): 505.3 & 507.2(M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(3,3-dimethylbutanamido)-1H-indazole-3-carboxamide(287a)

Compound 287a was prepared from5-amino-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(267e) (50 mg, 0.11 mmol) and 3,3-dimethylbutanoic acid (0.016 mL, 0.12mmol) according to the procedure reported in step-3 of Scheme 2. Thisgave after workup and purification by flash column chromatography[silica gel (4 g), eluting with dichloromethane/methanol (1:0 to 19:1)]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(3,3-dimethylbutanamido)-1H-indazole-3-carboxamide(287a) (50 mg, 83%). ¹H NMR (300 MHz, DMSO-d₆) δ 9.91 (s, 1H), 8.50 (t,J=5.8 Hz, 1H), 8.45-8.44 (m, 1H), 7.66 (s, 1H), 7.64-7.53 (m, 2H), 7.45(td, J=7.6, 1.7 Hz, 1H), 7.35 (s, 1H), 7.23 (td, J=7.2, 6.7, 1.7 Hz,1H), 7.11 (td, J=7.8, 1.0 Hz, 1H), 5.62 (s, 2H), 4.33 (d, J=5.7 Hz, 2H),3.98 (s, 2H), 3.13-2.97 (m, 1H), 2.20 (s, 2H), 1.04 (s, 9H), 1.02-0.85(m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.59; MS (ES+): 571.5 (M+1);593.5 & 595.5 (M+Na).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-N6-methyl-1H-indazole-3,6-dicarboxamide(288a)

Compound 288a was prepared from3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-6-carboxylicacid (208a) (50 mg, 0.1 mmol) and methanamine hydrochloride (10 mg, 0.15mmol) according to the procedure reported in step-3 of Scheme 2. Thisgave after workup and purification by flash column chromatography[silica gel (4 g), eluting with dichloromethane/methanol (1:0 to 19:1)]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-N6-methyl-1H-indazole-3,6-dicarboxamide(288a) (12 mg, 23%) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 8.56(t, J=5.7 Hz, 1H), 8.50 (d, J=4.6 Hz, 1H), 8.20 (dd, J=8.5, 0.8 Hz, 1H),8.14-8.12 (m, 1H), 7.80 (s, 1H), 7.70 (dd, J=8.6, 1.3 Hz, 1H), 7.49-7.38(m, 2H), 7.25-7.17 (m, 1H), 7.10-7.04 (m, 1H), 5.73 (s, 2H), 4.33 (d,J=5.7 Hz, 2H), 4.00 (s, 2H), 3.18-3.03 (m, 1H), 2.80 (d, J=4.5 Hz, 3H),1.09-0.78 (m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.62; MS (ES−): 549.3& 551.5 (M+Cl).

Preparation ofN-(1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-3-(1-hydroxyethyl)-1H-indazol-5-yl)-3,3-difluoropiperidine-1-carboxamide (289a)

To a suspension ofN-(3-acetyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazol-5-yl)-3,3-difluoropiperidine-1-carboxamide(239b) (50 mg, 0.08 mmol) in MeOH (10 mL) was added sodium borohydride(12 mg, 0.32 mmol) and stirred for 1h at room temperature. The mixturewas extracted with ethyl acetate (3×30 mL), the organic layer werecombined, dried, filtered and concentrated in vacuum. The residueobtained was purified by flash column chromatography [silica (12 g),eluting with DMA80 in DCM from 0 to 40%] to affordN-(1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-3-(1-hydroxyethyl)-1H-indazol-5-yl)-3,3-difluoropiperidine-1-carboxamide(289a) (30 mg, 0.048 mmol, 60% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.64 (s, 1H), 8.45 (t, J=5.9 Hz, 1H), 7.95-7.85 (m, 1H),7.54-7.42 (m, 1H), 7.42-7.32 (m, 2H), 7.28-7.19 (m, 1H), 7.18-7.08 (m,1H), 5.46 (s, 2H), 5.33 (d, J=4.0 Hz, 1H), 5.10-4.96 (m, 1H), 4.34 (d,J=5.7 Hz, 2H), 3.97 (s, 2H), 3.81 (t, J=12.1 Hz, 2H), 3.52 (t, J=5.3 Hz,2H), 3.12-2.97 (m, 1H), 2.17-1.94 (m, 2H), 1.79-1.63 (m, 2H), 1.52 (d,J=6.5 Hz, 3H), 1.04-0.93 (m, 2H), 0.93-0.83 (m, 2H); ¹⁹F NMR (282 MHz,DMSO-d₆) δ −101.13, −121.65; MS (ES+): 643.5 (M+Na); (ES−): 619.5 (M−1).

Preparation of2-(3-acetyl-5-(2-oxopyrrolidin-1-yl)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(290a)

Compound 290a was prepared from2-(3-acetyl-5-(2-oxopyrrolidin-1-yl)-1H-indol-1-yl)acetic acid (281b)(138 mg, 0.33 mmol) andN-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide (10b) (128 mg,0.5 mmol) according to the procedure reported in step-3 of Scheme 2.This gave after workup and purification by flash column chromatography[silica gel (24 g), eluting with ethyl acetate/methanol (9:1) in hexanes0-100%]]2-(3-acetyl-5-(2-oxopyrrolidin-1-yl)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(290a) (26 mg, 0.05 mmol, 14% yield) as an off-white solid; ¹H NMR (300MHz, DMSO-d₆) δ 8.47 (t, J=5.8 Hz, 1H), 8.29 (s, 1H), 8.25 (d, J=2.1 Hz,1H), 7.54 (dd, J=8.9, 2.1 Hz, 1H), 7.50-7.39 (m, 2H), 7.28-7.18 (m, 1H),7.15-7.04 (m, 1H), 5.43 (s, 2H), 4.35 (d, J=5.7 Hz, 2H), 3.99 (s, 2H),3.87 (t, J=7.0 Hz, 2H), 3.17-3.00 (m, 1H), 2.54-2.46 (m, 2H), 2.42 (s,3H), 2.09 (p, J=7.6 Hz, 2H), 1.02-0.85 (m, 4H); ¹⁹F NMR (282 MHz,DMSO-d₆) δ −121.63; MS (ES+): 539.5 (M+1), 561.5 (M+Na); MS (ES−): 537.4(M−1); 573.4 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(3,3-difluoropiperidine-1-carboxamido)-1H-pyrazolo[3,4-b]pyridine-3-carboxamide(291h) Step-1: Preparation of methyl1-(2-(tert-butoxy)-2-oxoethyl)-3-iodo-1H-pyrazolo[3,4-b]pyridine-5-carboxylate(291b)

Compound 291b was prepared from methyl3-iodo-1H-pyrazolo[3,4-b]pyridine-5-carboxylate (291a) (950 mg, 3.13mmol) according to the procedure reported in step-1 of Scheme 56. Thisgave after workup and purification by flash column chromatography[silica (24 g), eluting with hexanes/EtOAc (1:0 to 2:1)] methyl1-(2-(tert-butoxy)-2-oxoethyl)-3-iodo-1H-pyrazolo[3,4-b]pyridine-5-carboxylate(291b) (595 mg, 46% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ9.11 (d, J=2.0 Hz, 1H), 8.42 (d, J=2.0 Hz, 1H), 5.32 (s, 2H), 3.93 (s,3H), 1.40 (s, 9H); MS (ES+); 440.3 (M+Na).

Step-2: Preparation of methyl1-(2-(tert-butoxy)-2-oxoethyl)-3-cyano-1H-pyrazolo[3,4-b]pyridine-5-carboxylate(291c)

Compound 291c was prepared from methyl1-(2-(tert-butoxy)-2-oxoethyl)-3-iodo-1H-pyrazolo[3,4-b]pyridine-5-carboxylate(291b) (341 mg, 0.82 mmol) according to the procedure reported in step-3of Scheme 207. This gave after workup and purification by flash columnchromatography [silica (24 g), eluting with hexanes/EtOAc (1:0 to 3:1)]methyl1-(2-(tert-butoxy)-2-oxoethyl)-3-cyano-1H-pyrazolo[3,4-b]pyridine-5-carboxylate(291c) (188 mg, 73% yield) as a yellow solid; ¹H NMR (300 MHz, DMSO-d₆)δ 9.23 (d, J=1.9 Hz, 1H), 9.01 (d, J=1.9 Hz, 1H), 5.52 (s, 2H), 3.95 (s,3H), 1.40 (s, 9H); MS (ES+): 339.3 (M+Na).

Step-3: Preparation of 2-(3-cyano-5-(methoxycarbonyl)-1H-pyrazolo[3,4-b]pyri din-1-yl)acetic acid (291d)

Compound 291d was prepared from methyl1-(2-(tert-butoxy)-2-oxoethyl)-3-cyano-1H-pyrazolo[3,4-b]pyridine-5-carboxylate(291c) (293 mg, 0.93 mmol), according to the procedure reported instep-2 of Scheme 2. This gave after workup2-(3-cyano-5-(methoxycarbonyl)-1H-pyrazolo[3,4-b]pyridin-1-yl)aceticacid (291d) as a brown gum which was used as such without furtherpurification.

Step-4: Preparation of methyl1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-3-cyano-1H-pyrazolo[3,4-b]pyridine-5-carboxylate(291e)

Compound 291e was prepared from2-(3-cyano-5-(methoxycarbonyl)-1H-pyrazolo[3,4-b]pyridin-1-yl)aceticacid (291d) (241 mg, 0.93 mmol) andN-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide (10b) (285 mg,1.11 mmol) according to the procedure reported in step-3 of Scheme 2.This gave after workup and purification by flash column [silica (24 g),eluting with hexanes/10% methanol in ethyl acetate (1:0 to 1:1)] methyl1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-3-cyano-1H-pyrazolo[3,4-b]pyridine-5-carboxylate(291e) (338 mg, 73% yield) as a brown gum; ¹H NMR (300 MHz, DMSO-d₆) δ9.20 (d, J=1.9 Hz, 1H), 9.01 (d, J=1.9 Hz, 1H), 8.48 (t, J=5.8 Hz, 1H),7.51-7.40 (m, 1H), 7.29-7.06 (m, 2H), 5.86 (s, 2H), 4.32 (d, J=5.8 Hz,2H), 3.97 (s, 2H), 3.96 (s, 3H), 3.15-3.05 (m, 1H), 1.04-0.86 (m, 4H);¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.57; MS (ES+): 499.4 (M+1).

Step-5: Preparation of3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-pyrazolo[3,4-b]pyridine-5-carboxylicacid (291f)

Compound 291f was prepared from methyl1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-3-cyano-1H-pyrazolo[3,4-b]pyridine-5-carboxylate(291e) (326 mg, 0.65 mmol) according to the procedure reported in step-4of Scheme 43. This gave after workup

3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-pyrazolo[3,4-b]pyridine-5-carboxylicacid (291f) (200 mg, 61% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 9.09 (d, J=2.0 Hz, 1H), 9.06 (d, J=2.0 Hz, 1H), 8.51 (t,J=5.8 Hz, 1H), 8.05 (s, 1H), 7.68 (s, 1H), 7.49-7.42 (m, 1H), 7.26-7.18(m, 1H), 7.12 (td, J=7.8, 1.0 Hz, 1H), 5.73 (s, 2H), 4.31 (d, J=5.5 Hz,2H), 3.98 (s, 2H), 3.16-2.98 (m, 1H), 1.03-0.85 (m, 4H); ¹⁹F NMR (282MHz, DMSO-d₆) δ −121.56; MS (ES+): 503.4 (M+1); 525.4 and 527.4 (M+Na).

Step-6: Preparation of3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-pyrazolo[3,4-b]pyridine-5-carbonylazide (291g)

Compound 291g was prepared from3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-pyrazolo[3,4-b]pyridine-5-carboxylicacid (291f) (100 mg, 0.2 mmol) according to the procedure reported instep-3 of Scheme 129. This gave after work up3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-pyrazolo[3,4-b]pyridine-5-carbonylazide (291g) which was used as such without further purification.

Step-7: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(3,3-difluoropiperidine-1-carboxamido)-1H-pyrazolo[3,4-b]pyridine-3-carboxamide (291h)

Compound 291h was prepared from3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-pyrazolo[3,4-b]pyridine-5-carbonylazide (291g) (105 mg, 0.2 mmol) and 3,3-difluoropiperidine hydrochloride(63 mg, 0.4 mmol) using TEA (0.11 mL, 0.8 mmol) as base according to theprocedure reported in step-4 of Scheme 129 to afford after workup andpurification by column chromatography [silica gel (8 g), eluting withDCM in methanol (1:0 to 9:1)]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(3,3-difluoropiperidine-1-carboxamido)-1H-pyrazolo[3,4-b]pyridine-3-carboxamide(291h) (15 mg, 12% yield for two steps) as a white solid; ¹H NMR (300MHz, DMSO-d₆) δ 8.99 (s, 1H), 8.67 (d, J=2.4 Hz, 1H), 8.59 (d, J=2.4 Hz,1H), 8.51 (t, J=5.8 Hz, 1H), 7.83 (s, 1H), 7.53-7.41 (m, 2H), 7.28-7.17(m, 1H), 7.16-7.08 (m, 1H), 5.65 (s, 2H), 4.32 (d, J=5.7 Hz, 2H), 3.98(s, 2H), 3.84 (t, J=12.1 Hz, 2H), 3.60-3.52 (m, 2H), 3.13-3.00 (m, 1H),2.19-1.93 (m, 2H), 1.81-1.61 (m, 2H), 1.04-0.75 (m, 4H); ¹⁹F NMR (282MHz, DMSO-d₆) δ −101.19, −121.59; MS (ES+): 643.5 (M+Na); (ES−): 655.5and 657.5 (M+Cl).

Preparation of(R)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-hydroxybutan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(292d) Step-1: Preparation of(R)-2-((1-((tert-butyldimethylsilyl)oxy)butan-2-yl)-amino)-N-(3-chloro-2-fluorobenzyl)acetamide(292b)

Compound 292b was prepared according to the procedure reported in step-2of Scheme 35 from 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b)(300 mg, 1.27 mmol) and(R)-1-((tert-butyldimethylsilyl)oxy)butan-2-amine (292a) (284 mg, 1.4mmol, prepared according to the procedure reported by Gant, Thomas G.and Sarshar, Sepehr; in PCT Int. Appl., 2009032843). This gave gaveafter workup(R)-2-((1-((tert-butyldimethylsilyl)oxy)butan-2-yl)amino)-N-(3-chloro-2-fluorobenzyl)acetamide(292b) as a colorless oil which was used as such in the next step; MS(ES+): 403.4 (M+1); MS (ES−): 401.4 (M−1), 437.4 (M+Cl).

Step-2: Preparation of(R)-1-(2-((1-((tert-butyldimethylsilyl)oxy)butan-2-yl)(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(292c)

Compound 292c was prepared from(R)-2-((1-((tert-butyldimethylsilyl)oxy)butan-2-yl)amino)-N-(3-chloro-2-fluorobenzyl)acetamide(292b) (300 mg, 0.74 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (163 mg, 0.74 mmol) according to the procedure reported instep-3 of Scheme 2. This gave after workup and purification by flashcolumn chromatography [silica (24 g), eluting with methanol in DCM from0-20%](R)-1-(2-((1-((tert-butyldimethylsilyl)oxy)butan-2-yl)(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(292c) (171 mg, 38% yield) as a white solid; MS (ES+): 604.5 (M+1);626.5 (M+Na); MS (ES−): 602.5 (M−1).

Step-3: Preparation of(R)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-hydroxybutan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(292d)

To a stirred solution of(R)-1-(2-((1-((tert-butyldimethylsilyl)oxy)butan-2-yl)(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(292c) (162 mg, 0.27 mmol) in MTBE (10 mL) was added at room temperatureconc. HCl (0.223 mL, 2.68 mmol) and stirred for 1 h. The reaction wasconcentrated in vacuum to dryness basified with saturated aqueous NaHCO₃and extracted with ethyl acetate (2×50 mL). The organic layers werecombined dried, filtered and evaporated to dryness. The residue obtainedwas purified by flash column chromatography [First column, silica gel,(12 g) eluting with ethyl acetate/methanol (9:1) in hexanes from 0-100%;second column, Silica gel, (12 g) eluting with methanol in DCM from0-10%)) to afford(R)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-hydroxybutan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(292d) (18 mg, 0.04 mmol, 14% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.92 (t, J=5.7 Hz) & 8.72 (t, J=5.9 Hz) (2t, 1H), 8.26-8.13(m, 1H), 7.77 & 7.72 (2s, 1H), 7.56-6.93 (m, 7H), 5.71-3.89 (m) (6H),4.24 and 3.86 (2s, 2H), 3.65-3.33 (m, 2H), 1.58-1.40 (m, 2H), 0.96 (t,J=7.3 Hz) & 0.75 (t, J=7.3 Hz) (2t, 3H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.27, −121.59; MS (ES+): 490.4, 492.4 (M+1); MS (ES−): 488.4, 490.3(M−1), 524.4, 526.4 (M+Cl).

Preparation of2-(3-acetyl-5-(3-methyl-3-(1-methylpiperidin-4-yl)ureido)-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(293a)

Compound 293a was prepared from3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (217a) (500 mg, 0.95 mmol) and N,1-dimethylpiperidin-4-amine (243mg, 1.9 mmol), using TEA (0.26 mL, 1.9 mmol) as base according to theprocedure reported in step-4 of Scheme 129. This gave after workup,purification by flash column chromatography [silica gel (12g), elutingwith DMA80 in DCM 0 to 40%]2-(3-acetyl-5-(3-methyl-3-(1-methylpiperidin-4-yl)ureido)-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-isopropylacetamide(293a) (38 mg, 7% yield) white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 8.83(t, J=5.7 Hz) and 8.35 (t, J=5.8 Hz) (2t, 1H), 8.44 (s, 1H), 8.26-8.20(m, 1H), 7.64-7.55 (m, 1H), 7.54-7.00 (m, 4H), 5.63 and 5.47 (2s, 2H),4.62-4.52 and 4.28-4.24 (2m, 1H), 4.47 (d, J=5.6 Hz) and 4.32 (d, J=5.9Hz) (2d, 2H), 4.17 and 3.85 (2s, 2H), 4.13-3.96 (m, 1H), 2.59 (s, 3H),2.17 (s, 3H), 2.87-2.79 and 2.01-1.90 and 1.80-1.64 and 1.56-1.46 (4m,11H), 1.24 (d, J=6.3 Hz) and 1.00 (d, J=6.8 Hz) (2d, 6H); ¹⁹F NMR (282MHz, DMSO-d₆) δ −121.22, −121.78; MS (ES+) 628.7 (M+1); (ES−) 626.6(M−1).

Preparation of (5)-tert-butyl(1-((3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazol-5-yl)carbamoyl)piperidin-3-yl)carbamate(294a)

Compound 294a was prepared from3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (235a) (750 mg, 0.71 mmol) and (5)-tert-butylpiperidin-3-ylcarbamate (285 mg, 1.423 mmol), using TEA (0.2 mL, 1.4mmol) as base according to the procedure reported in step-4 of Scheme129. This gave after workup, purification by flash column chromatography[silica gel (12g), eluting with DMA80 in DCM 0 to 40%] followed bypreparative HPLC [C₁₈ column, eluting with CH₃CN in water 0-100%](S)-tert-butyl(1-((3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazol-5-yl)carbamoyl)piperidin-3-yl)carbamate(294a) (86 mg, 17% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ8.65 (s, 1H), 8.50 (t, J=5.8 Hz, 1H), 8.20-8.14 (m, 1H), 7.63 (s, 1H),7.59-7.42 (m, 3H), 7.31 (s, 1H), 7.28-7.19 (m, 1H), 7.19-7.07 (m, 1H),6.97-6.85 (m, 1H), 5.61 (s, 2H), 4.33 (d, J=5.7 Hz, 2H), 4.08-3.86 (m,4H), 3.44-3.24 (m, 3H), 3.11-2.99 (m, 1H), 2.86-2.59 (m, 2H), 1.90-1.77(m, 1H), 1.77-1.64 (m, 1H), 1.38 (s, 9H), 1.04-0.96 (m, 2H), 0.96-0.83(m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −73.73 (TFA peak), −121.62; MS(ES+) 699.7 (M+1); (ES−) 697.7 (M−1).

Preparation of 2-(3-acetyl-5-(pyrimidin-5-yl)-1H-pyrrolo[2,3-c]pyridin-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(295e) Step-1: Preparation of ethyl2-(3-acetyl-5-bromo-1H-pyrrolo[2,3-c]pyridin-1-yl)acetate (295b)

Compound 295b was prepared according to the procedure reported in step-1of Scheme 56 from 1-(5-bromo-1H-pyrrolo[2,3-c]pyridin-3-yl)ethanone(295a) (1.2 g, 5.02 mmol, prepared according to procedure reported byHynd, George et al: in PCT Int. Appl., 2014174021). This gave afterworkup and purification by flash column chromatography [silica (24 g),eluting with DMA80 in DCM 0 to 30%] ethyl2-(3-acetyl-5-bromo-1H-pyrrolo[2,3-c]pyridin-1-yl)acetate (295b) (850mg, 52% yield) as a light orange solid; ¹H NMR (300 MHz, DMSO-d₆) δ 8.79(d, J=1.0 Hz, 1H), 8.58 (s, 1H), 8.18 (d, J=0.9 Hz, 1H), 5.36 (s, 2H),4.19 (q, J=7.1 Hz, 2H), 2.46 (s, 3H), 1.23 (t, J=7.1 Hz, 3H); MS (ES+)325.3, 327.3 (M+1), 347.3, 349.3 (M+Na): MS (ES−): 359.2, 361.2 (M+Cl).

Step-2: Preparation of2-(3-acetyl-5-bromo-1H-pyrrolo[2,3-c]pyridin-1-yl)acetic acid (295c)

Compound 295c was prepared from ethyl2-(3-acetyl-5-bromo-1H-pyrrolo[2,3-c]pyridin-1-yl)acetate (295b) (500mg, 1.54 mmol) according to the procedure reported in step-2 of Scheme129. This gave after workup2-(3-acetyl-5-bromo-1H-pyrrolo[2,3-c]pyridin-1-yl)acetic acid (295c)(260 mg, 0.88 mmol, 57% yield) as a light orange solid; ¹H NMR (300 MHz,DMSO-d₆) δ 13.42 (s, 1H), 8.79 (d, J=0.9 Hz, 1H), 8.59 (s, 1H), 8.18 (d,J=0.9 Hz, 1H), 5.25 (s, 2H), 2.46 (s, 3H); MS (ES−): 295.1, 297.1 (M−1).

Step-3: Preparation of2-(3-acetyl-5-bromo-1H-pyrrolo[2,3-c]pyridin-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(295d)

Compound 295d was prepared from2-(3-acetyl-5-bromo-1H-pyrrolo[2,3-c]pyridin-1-yl)acetic acid (295c)(250 mg, 0.84 mmol) withN-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide (10b) (259 mg,1.01 mmol) according to the procedure reported in step-3 of Scheme 2.This gave after workup and purification by flash column [silica gel (12g), eluting with DMA80-DCM 0 to 20%]2-(3-acetyl-5-bromo-1H-pyrrolo[2,3-c]pyridin-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(295d) (70 mg, 15% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ8.68 (s, 1H), 8.53 (s, 1H), 8.47 (t, J=6.0 Hz, 1H), 8.18 (d, J=0.9 Hz,1H), 7.52-7.41 (m, 1H), 7.27-7.18 (m, 1H), 7.14-7.04 (m, 1H), 5.57 (s,2H), 4.34 (d, J=5.8 Hz, 2H), 3.99 (s, 2H), 3.14-3.03 (m, 1H), 2.46 (s,3H), 1.05-0.94 (m, 2H), 0.95-0.86 (m, 2H); 19F NMR (282 MHz, DMSO-d₆) δ−121.59; MS (ES+) 535.4, 537.4 (M+1); MS (ES−): 569.3, 571.3 (M+Cl).

Step-4: Preparation of Preparation of2-(3-acetyl-5-(pyrimidin-5-yl)-1H-pyrrolo[2,3-c]pyridin-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(295e)

Compound 295e was prepared according from to2-(3-acetyl-5-bromo-1H-pyrrolo[2,3-c]pyridin-1-yl-N-(2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(295d) (65 mg, 0.12 mmol) according to the procedure reported in Scheme92. This gave after workup and purification by flash column [silica gel(12 g), eluting with DMA80-DCM 0 to 20%]2-(3-acetyl-5-(pyrimidin-5-yl)-1H-pyrrolo[2,3-c]pyridin-1-yl)-N-(2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)-N-cyclopropylacetamide(295e) (55 mg, 0.1 mmol, 85% yield) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) 9.41 (s, 2H), 9.21 (s, 1H), 9.00 (d, J=1.1 Hz, 1H), 8.64 (d,J=1.1 Hz, 1H), 8.54 (s, 1H), 8.49 (t, J=5.8 Hz, 1H), 7.43 (td, J=7.7,7.2, 1.7 Hz, 1H), 7.28-7.19 (m, 1H), 7.14-7.02 (m, 1H), 5.64 (s, 2H),4.35 (d, J=5.7 Hz, 2H), 4.02 (s, 2H), 3.18-3.06 (m, 1H), 2.52 (s, 3H),1.08-0.98 (m, 2H), 0.98-0.88 (m, 2H); 19F NMR (282 MHz, DMSO-d₆) δ−121.59; MS (ES+): 535.5 (M+1), MS (ES−): 569.4 (M+Cl).

Preparation of(S)-1-(2-((2-((1-(3-chloro-2-fluorophenyl)ethyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-pyrazolo[3,4-c]pyridine-3-carboxamide(296f) Step-1: Preparation of2-(3-cyano-1H-pyrazolo[3,4-c]pyridin-1-yl)acetic acid (296b)

Compound 296b was prepared from tert-butyl2-(3-cyano-1H-pyrazolo[3,4-c]pyridin-1-yl)acetate (296a) (995 mg, 3.85mmol, prepared according to the procedure reported by Altmann, Eva etal; in PCT Int. Appl., 2014002058, 3 Jan. 2014) using TFA (2.5 mL, 2.66mmol) in CH₂Cl₂ (30 mL) according to the procedure reported in step-2 ofScheme 2. This gave after workup2-(3-cyano-1H-pyrazolo[3,4-c]pyridin-1-yl)acetic acid (296b) (1.78 g) asa brown gum which was used as such for next step.

Step-2: Preparation of ethyl2-(2-(3-cyano-1H-pyrazolo[3,4-c]pyridin-1-yl)-N-cyclopropylacetamido)acetate(296c)

Reaction of 2-(3-cyano-1H-pyrazolo[3,4-c]pyridin-1-yl)acetic acid (296b)(389 mg, 1.93 mmol) with ethyl 2-(cyclopropylamino)acetate (45b) (413mg, 2.89 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column chromatography[silica gel, eluting with dichloromethane/methanol (1:0 to 19:1)] ethyl2-(2-(3-cyano-1H-pyrazolo[3,4-c]pyridin-1-yl)-N-cyclopropylacetamido)acetate(296c) (317 mg, 50%) as a brown gum; ¹H NMR (300 MHz, DMSO-d₆) δ 9.31(s, 1H), 8.49 (d, J=5.8 Hz, 1H), 7.96 (d, J=5.7 Hz, 1H), 6.00 (s, 2H),4.18-3.99 (m, 4H), 3.20-3.03 (m, 1H), 1.18 (t, J=7.2 Hz, 3H), 0.98 (dd,J=27.3, 5.5 Hz, 4H); MS (ES+): 350.2 (M+Na).

Step-3: Preparation of2-(2-(3-carbamoyl-1H-pyrazolo[3,4-c]pyridin-1-yl)-N-cyclopropylacetamido)aceticacid (296d)

To a solution of ethyl2-(2-(3-cyano-1H-pyrazolo[3,4-c]pyridin-1-yl)-N-cyclopropylacetamido)acetate(296c) (308 mg, 0.941 mmol) in THF (20 mL) and MeOH (20.00 mL) was addeda solution of lithium hydroxide hydrate (242 mg, 5.65 mmol) in water (20mL) and stirred at RT for 15 h. The reaction mixture was concentrated toremove THF and methanol. The residue was treated with water (15 mL) andacidified carefully with 4 N HCl followed by concentration to dryness togive2-(2-(3-carbamoyl-1H-pyrazolo[3,4-c]pyridin-1-yl)-N-cyclopropylacetamido)aceticacid (296d) (660 mg) as a brown gum which was used as such for nextstep; MS (ES−): 316.2 (M−1).

Step-4: Preparation of(5)-1-(2-((2-((1-(3-chloro-2-fluorophenyl)ethyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-pyrazolo[3,4-c]pyridine-3-carboxamide(296f)

Reaction of2-(2-(3-carbamoyl-1H-pyrazolo[3,4-c]pyridin-1-yl)-N-cyclopropylacetamido)aceticacid (296d) (102 mg, 0.32 mmol) with(S)-1-(3-chloro-2-fluorophenyl)ethanamine hydrochloride (296e) (70.8 mg,0.320 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column chromatography[silica gel, eluting with dichloromethane/methanol (1:0 to 9:1)](S)-1-(2-((2-((1-(3-chloro-2-fluorophenyl)ethyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-pyrazolo[3,4-c]pyridine-3-carboxamide(296f) (24 mg, 16% for two steps) as a yellow solid; ¹H NMR (300 MHz,DMSO-d₆) δ 9.15 (s, 1H), 8.59 (d, J=7.4 Hz, 1H), 8.35 (d, J=5.5 Hz, 1H),8.05 (d, J=5.7 Hz, 1H), 7.95 (s, 1H), 7.54 (s, 1H), 7.44 (t, J=7.5 Hz,1H), 7.28 (t, J=7.3 Hz, 1H), 7.14 (t, J=7.9 Hz, 1H), 5.79 (s, 2H),5.15-4.96 (m, 1H), 3.99 (s, 2H), 3.08-2.94 (m, 1H), 1.33 (d, J=7.0 Hz,3H), 1.04-0.82 (m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −122.71; MS (ES+):495.1 & 497.1 (M+Na); MS (ES−): 471.2 (M−1) & 507.1 (M+Cl).

Preparation of3-acetyl-N-benzyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-4-carboxamide(297a)

Reaction of3-acetyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-4-carboxylicacid (284g) (50 mg, 0.10 mmol) with phenylmethanamine (0.017 mL, 0.15mmol) according to the procedure reported in step-3 of Scheme 2 gaveafter workup and purification by flash column chromatography [silicagel, eluting with hexanes/10% methanol in ethyl acetate, 1:0 to 1:2]3-acetyl-N-benzyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-4-carboxamideas a white solid (297a) (21 mg, 36%). ¹H NMR (300 MHz, DMSO-d₆) δ 8.73(t, J=5.9 Hz, 1H), 8.48 (t, J=5.9 Hz, 1H), 7.75 (dd, J=8.6, 0.9 Hz, 1H),7.52-7.18 (m, 9H), 7.10 (td, J=7.9, 1.0 Hz, 1H), 5.77 (s, 2H), 4.50 (d,J=5.9 Hz, 2H), 4.34 (d, J=5.7 Hz, 2H), 3.99 (s, 2H), 3.19-3.05 (m, 1H),2.58 (s, 3H), 1.09-0.84 (m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.61;MS(ES+): 612.5 & 614.5 (M+Na); MS (ES−): 624.5 & 626.5 (M+Cl).

Preparation of3-acetyl-1-(2-((2-(2′-chloro-2-fluorobiphenyl-3-ylamino)-2-oxoethyl)(isopropyl)-amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (298b) Step 1: Preparation of methyl3-acetyl-1-(2-((2-(2′-chloro-2-fluorobiphenyl-3-ylamino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylate(298a)

Reaction of 2-(3-acetyl-5-(methoxycarbonyl)-1H-indazol-1-yl)acetic acid(206c) (2.35 g, 8.51 mmol) withN-(2′-chloro-2-fluorobiphenyl-3-yl)-2-(isopropylamino)acetamide (19c)(2.1 g, 6.55 mmol according to the procedure reported in step-3 ofScheme 2 gave crude product. The crude product was stirred with 50%EtOAc-hexane (50 mL) and solid obtained was collected by filtration,washed with EtOAc (2×1 mL) to afford methyl3-acetyl-1-(2-((2-(2′-chloro-2-fluorobiphenyl-3-ylamino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylate(298a) (3.0 g, 79% yield) as an off-white solid. ¹H NMR (300 MHz,DMSO-d₆) (a mixture of rotamers) δ 10.27 and 9.74 (2s, 1H), 8.85 and8.83 (2dd, J=1.6, 0.8 Hz, 1H), 8.16-8.09 and 7.98-7.90 (2m, 1H), 8.07and 8.02 (2dd, J=8.9, 1.6 Hz, 1H), 7.83-6.99 (m, 7H), 5.82 and 5.64 (2s,2H), 4.69-4.57 and 4.38-4.27 (2m, 1H), 4.47 and 4.09 (2s, 2H), 3.912 and3.906 (2s, 3H), 2.65 and 2.64 (2s, 3H), 1.29 and 1.07 (2d, J=6.8 Hz,6H); MS (ES+) 579.5 (M+1), MS(ES−) 613.6 (M+Cl).

Step 2: preparation of3-acetyl-1-(2-((2-(2′-chloro-2-fluorobiphenyl-3-ylamino)-2-amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (298b)

Reaction of methyl3-acetyl-1-(2-((2-(2′-chloro-2-fluorobiphenyl-3-ylamino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylate (298a) (3 g, 5.18 mmol)with lithium hydroxide (0.37 g, 15.54 mmol) according to the procedurereported in step-2 of Scheme 129 gave after workup and purification3-acetyl-1-(2-((2-(2′-chloro-2-fluorobiphenyl-3-ylamino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (298b) (2.75 g, 94% yield) as a white solid. ¹H NMR (300 MHz,DMSO-d₆) δ 13.05 (s, 1H), 10.28 and 9.75 (2s, 1H), 8.83 and 8.81 (2dd,J=1.6, 0.8 Hz, 1H), 8.1-6.98 (m, 9H), 5.81 and 5.63 (2s, 2H), 4.70-4.57and 4.39-4.26 (2m, 1H), 4.47 and 4.09 (2s, 2H), 2.65 and 2.64 (2s, 3H),1.29 and 1.07 (2d, J=6.8 Hz, 6H); 19F NMR (282 MHz, DMSO-d₆) δ −126.84,−126.96; MS(ES−) 563.5 (M−1), 599.5 (M+Cl).

Preparation of (R)-tert-butyl1-(3-carbamoyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)-amino)-2-oxoethyl)-1H-indazol-5-ylcarbamoyl)piperidin-3-ylcarbamate(299a)

Reaction of3-carbamoyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (235a) (750 mg, 0.712 mmol) with (R)-tert-butylpiperidin-3-ylcarbamate (285 mg, 1.42 mmol) according to the procedurereported in step-4 of Scheme 129 gave after workup and purification byflash column chromatography [silica (12g), eluting with 0 to 40% DMA-80in DCM] and preparative HPLC [C₁₈ column, eluting with CH₃CN in waterfrom 0-100%] (R)-tert-butyl1-(3-carbamoyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazol-5-ylcarbamoyl)piperidin-3-ylcarbamate(299a) (75 mg, 15% yield) as a white solid. ¹H NMR (300 MHz, DMSO-d₆) δ8.65 (s, 1H), 8.50 (t, J=5.8 Hz, 1H), 8.23-8.12 (m, 1H), 7.63 (s, 1H),7.58-7.42 (m, 3H), 7.31 (s, 1H), 7.27-7.23 (m, 1H), 7.13 (t, J=7.8 Hz,1H), 6.91 (d, J=7.9 Hz, 1H), 5.61 (s, 2H), 4.33 (d, J=5.7 Hz, 2H),4.12-3.84 (m, 4H), 3.42-3.21 (m, 1H), 3.12-2.99 (m, 1H), 2.87-2.58 (m,2H), 1.90-1.59 (m, 2H), 1.48-1.28 (m, 11H), 1.09-0.96 (m, 2H), 0.96-0.81(m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −74.22 (TFA peak), −121.62; MS(ES+) 699.7 (M+1); (ES−) 697.7 (M−1).

Preparation of1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(3-methyl-3-(1-methylazetidin-3-yl)ureido)-1H-indazole-3-carboxamide(300a)

Reaction3-carbamoyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (235a) (500 mg, 0.47 mmol) with N,1-dimethylazetidin-3-amine (86mg, 0.85 mmol) according to the procedure reported in step-4 of Scheme129 gave after workup and purification by chromatography [silica (40g),eluting with 0 to 40% DMA80 in DCM], then [silica (24 g), eluting with 0to 90% EtOAc/MeOH (9:1) in hexane] and prep-HPLC [C₁₈ column, 5injections, eluting with CH₃CN in water (containing 0.1% TFA) from0-100%], followed by lyophilization1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(3-methyl-3-(1-methylazetidin-3-yl)ureido)-1H-indazole-3-carboxamide(300a) (65 mg, 26% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ8.86 (s, 1H), 8.75 (s, 1H), 8.53 (t, J=5.8 Hz, 1H), 8.16 (s, 1H), 7.82(s, 1H), 7.72 (d, J=9.0 Hz, 1H), 7.52-7.41 (m, 2H), 7.41-7.31 (m, 1H),7.27-7.19 (m, 1H), 7.18-7.08 (m, 1H), 5.68 (s, 2H), 4.93-4.69 (m, 2H),4.51-4.37 (m, 1H), 4.33 (d, J=5.7 Hz, 2H), 3.99 (s, 2H), 3.49-3.31 (m,2H), 3.18 (s, 3H), 3.11-3.00 (m, 1H), 2.68 (s, 3H), 1.03-0.96 (m, 2H),0.96-0.87 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −73.80 (TFA peak),−121.54; MS (ES⁺) 599.6 (M+1); (ES−) 597.5 (M−1).

Preparation of1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-6-(cyanomethoxy)-1H-indazole-3-carboxamide(301h) Step 1: Preparation of tert-butyl2-(6-(tert-butyldimethylsilyloxy)-3-iodo-1H-indazol-1-yl)acetate (301b)

Reaction of 6-(tert-butyldimethylsilyloxy)-3-iodo-1H-indazole (301a)(36.2 mmol, crude prepared according to the procedure reported by Atobe,Masakazu et al; in Bioorganic Medicinal Chemistry Letters, 24(5),1327-1333; 201.4) with tert-butyl 2-bromoacetate (6.41 mL, 43.4 mmol)according to the procedure reported in step-1 of Scheme 43 gave afterworkup and purification tert-butyl2-(6-(tert-butyldimethylsilyloxy)-3-iodo-1H-indazol-1-yl)acetate as abrown gum (301b) (17.25 g, used as such for next step). MS (ES+): 489.4(M+1).

Step 2: Preparation of tert-butyl2-(6-hydroxy-3-iodo-1H-indazol-1-yl)acetate (301c)

To a solution of tert-butyl2-(6-(tert-butyldimethylsilyloxy)-3-iodo-1H-indazol-1-yl)acetate (301d)(17.68 g, crude) in THF (200 mL) cooled to 0° C. was addedtetrabutylammonium fluoride (10.96 g, 39.8 mmol) and stirred at RT for 6h. The reaction mixture was poured into ice-water (300 mL), extractedwith ethyl acetate (300, 200 mL). The combined organic extracts werewashed with brine (300 mL), dried, filtered and concentrated in vacuum.The crude product was purified by flash column chromatography [silicagel, eluting with hexanes/EtOAc (1:0 to 3:1)] to give tert-butyl2-(6-hydroxy-3-iodo-1H-indazol-1-yl)acetate as a yellow solid (301c)(7.61 g, 56% for 4 steps). ¹H NMR (300 MHz, DMSO-d₆) δ 9.94 (s, 1H),7.21 (dd, J=8.6, 0.7 Hz, 1H), 6.80-6.79 (m, 1H), 6.76 (dd, J=8.6, 1.9Hz, 1H), 5.13 (s, 2H), 1.41 (s, 9H); MS(ES+): 397.2 (M+Na).

Step 3: Preparation of tert-butyl2-(3-cyano-6-hydroxy-1H-indazol-1-yl)acetate (301d)

A mixture of tert-butyl 2-(6-hydroxy-3-iodo-1H-indazol-1-yl)acetate(301c) (3.1 g, 8.28 mmol), dicyanozinc (1.07 g, 9.11 mmol), Pd₂(dba)₃(0.76 g, 0.83 mmol), and[1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium(II), complexwith dichloromethane (Pd(dppf)Cl₂.CH₂Cl₂) (0.68 g, 0.83 mmol) in DMF (35mL) and water (3.5 mL) was stirred at 80° C. for 3 h. The reactionmixture was diluted with ethyl acetate (200 mL), washed with water (80mL), Sat. NaHCO₃ (60 mL) and brine (50 mL), dried, filtered andconcentrated in vacuum. The crude product was purified by flash columnchromatography [silica gel, eluting with hexanes/ethyl acetate (1:0 to3:1)] to give tert-butyl 2-(3-cyano-6-hydroxy-1H-indazol-1-yl)acetate asa yellow solid (301d) (880 mg, 39%); ¹H NMR (300 MHz, DMSO-d₆) δ 10.27(s, 1H), 7.69 (dd, J=8.7, 0.7 Hz, 1H), 7.00-6.98 (m, 1H), 6.96 (dd,J=8.7, 2.0 Hz, 1H), 5.34 (s, 2H), 1.41 (s, 9H); MS(ES+): 296.3 (M+Na).

Step 4: Preparation of tert-butyl2-(3-carbamoyl-6-hydroxy-1H-indazol-1-yl)acetate (301e)

A mixture of tert-butyl 2-(3-cyano-6-hydroxy-1H-indazol-1-yl)acetate(301d) (858 mg, 3.14 mmol), palladium (II) acetate (71.9 mg, 0.31 mmol),triphenylphosphine (166 mg, 0.63 mmol), and acetaldehyde oxime (0.39 mL,6.28 mmol) in ethanol (20 mL) and water (5 mL) was refluxed for 3 h. Thereaction mixture was cooled to RT, diluted with ethyl acetate (60 mL),filtered and concentrated in vacuum. The crude product was purified byflash column chromatography [silica gel, eluting with hexanes/ethylacetate (1:0 to 0:1)] to give tert-butyl2-(3-carbamoyl-6-hydroxy-1H-indazol-1-yl)acetate as a white solid (301e)(749 mg, 82%). MS (ES−): 290.3 (M −1).

Step 5: Preparation of tert-butyl2-(3-carbamoyl-6-(cyanomethoxy)-1H-indazol-1-yl)acetate (301f)

A suspension of tert-butyl2-(3-carbamoyl-6-hydroxy-1H-indazol-1-yl)acetate (301e) (100 mg, 0.34mmol) in DMF (5 mL) was treated with Potassium carbonate (96 mg, 0.69mmol) and 2-bromoacetonitrile (0.025 mL, 0.34 mmol) followed by stirringat RT for 13 h. The reaction mixture was diluted with ethyl acetate (100mL), washed with water (2×50 mL), brine (50 mL), dried, filtered andconcentrated in vacuum to give tert-butyl2-(3-carbamoyl-6-(cyanomethoxy)-1H-indazol-1-yl)acetate as a yellowsolid (301f) (107 mg, used as such for next step). MS(ES+): 353.3(M+Na).

Step 6: Preparation of2-(3-carbamoyl-6-(cyanomethoxy)-1H-indazol-1-yl)acetic acid (301g)

Reaction of tert-butyl2-(3-carbamoyl-6-(cyanomethoxy)-1H-indazol-1-yl)acetate (301f) (0.113 g,0.34 mmol, crude) with 2,2,2-trifluoroacetic acid (0.264 mL, 3.43 mmol)according to the procedure reported in step-2 of Scheme 2 gave afterworkup and purification2-(3-carbamoyl-6-(cyanomethoxy)-1H-indazol-1-yl)acetic acid (301g) whichwas used as such for next step.

Step 7: Preparation of1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-6-(cyanomethoxy)-1H-indazole-3-carboxamide(301h)

Reaction of 2-(3-carbamoyl-6-(cyanomethoxy)-1H-indazol-1-yl)acetic acid(301g) (0.094 g, 0.34 mmol, crude) withN-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide (0.11 g, 0.41mmol) (10b) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column chromatography[silica gel, eluting with dichloromethane/methanol (1:0 to 19:1)]1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-6-(cyanomethoxy)-1H-indazole-3-carboxamide(301h) (44 mg, 25% for 3 steps) as a light brown solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.54 (t, J=5.8 Hz, 1H), 8.10 (d, J=8.9 Hz, 1H), 7.72 (s, 1H),7.52-7.33 (m, 2H), 7.29 (d, J=2.2 Hz, 1H), 7.26-7.18 (m, 1H), 7.14-7.04(m, 1H), 7.01 (dd, J=8.9, 2.2 Hz, 1H), 5.60 (s, 2H), 5.20 (s, 2H), 4.34(d, J=5.7 Hz, 2H), 4.00 (s, 2H), 3.13-2.98 (m, 1H), 1.06-0.84 (m, 4H);¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.56; MS(ES+): 513.5 & 515.5 (M+1); MS(ES−): 547.4 & 549.4 (M+Cl).

Preparation ofN-(3-acetyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(isopropyl)-amino)-2-oxoethyl)-1H-indazol-5-yl)-3,3-dimethylbutanamide(302d) Step-1: Preparation of3-acetyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(isopropyl)-amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (302a)

Reaction of3-acetyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (216a) (200 mg, 0.4 mmol) with diphenyl phosphorazidate (0.088 mL,0.4 mmol) according to the procedure reported in step-3 of Scheme 129gave after workup crude3-acetyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(isopropyl)-amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (302a), which was used as such for next step.

Step-2: Preparation of tert-butyl3-acetyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazol-5-ylcarbamate(302b)

Reaction of3-acetyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (302a) (210 mg, 0.4 mmol) with 2-methylpropan-2-ol (0.23 mL, 2.39mmol) according to the procedure reported in step-4 of Scheme 129 gaveafter workup and purification by flash column chromatography tert-butyl3-acetyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazol-5-ylcarbamate(302b) (20 mg, 9% for two steps) as a white solid; MS (ES+) 574.6, 575.6(M+1); (ES−) 572.6 (M−1); 608.5, 610.5 (M+Cl).

Step-3: Preparation of2-(3-acetyl-5-amino-1H-indazol-1-yl)-N-(2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)-N-isopropylacetamide(302c)

Reaction of tert-butyl3-acetyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazol-5-ylcarbamate(302b) (18 mg, 0.03 mmol) with 2,2,2-trifluoroacetic acid (0.193 mL,2.51 mmol) according to the procedure reported in step-2 of Scheme 2gave after workup crude2-(3-acetyl-5-amino-1H-indazol-1-yl)-N-(2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)-N-isopropylacetamide(302c), which was used as such for next step.

Step-4: Preparation ofN-(3-acetyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(isopropyl)-amino)-2-oxoethyl)-1H-indazol-5-yl)-3,3-dimethylbutanamide(302d)

Reaction of2-(3-acetyl-5-amino-1H-indazol-1-yl)-N-(2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)-N-isopropylacetamide(302c) (14.69 mg, 0.031 mmol) with 3,3-dimethylbutanoic acid (6.04 μL,0.047 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column chromatography[silica gel, eluting with hexanes/10% methanol in ethyl acetate (1:0 to1:1)]N-(3-acetyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazol-5-yl)-3,3-dimethylbutanamide(302d) (11 mg, 62% for two steps) as a light yellow solid; ¹H NMR (300MHz, DMSO-d₆) δ 9.97 (s, 1H), 8.83 (t, J=5.7 Hz) and 8.35 (t, J=5.8 Hz)(2t, 1H), 8.56-8.48 (m, 1H), 7.72-6.89 (m, 5H), 5.65 and 5.49 (2s, 2H),4.64-4.49 and 4.30-4.18 (2m, 1H), 4.47 (d, J=5.5 Hz) and 4.32 (d, J=5.8Hz) (2d, 2H), 4.17 and 3.84 (2s, 2H), 2.59 (s, 3H), 2.21 and 1.99 (2s,2H), 1.24 (d, J=6.3 Hz) and 0.99 (d, J=6.8 Hz) (2d, 6H), 1.04 and 1.04(2s, 9H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.22, −121.75; MS (ES+): 572.7(M+1).

Preparation ofN-(3-acetyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indol-5-yl)-3,3-dimethylbutanamide(303a)

Reaction of2-(3-acetyl-5-amino-1H-indol-1-yl)-N-(2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)-N-cyclopropylacetamide(286a) (14.36 mg, 0.031 mmol) with 3,3-dimethylbutanoic acid (5.95 μL,0.046 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column chromatography[silica gel, eluting with hexanes/10% methanol in ethyl acetate (1:0 to1:2)]N-(3-acetyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indol-5-yl)-3,3-dimethylbutanamide(303a) (11 mg, 63%) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 9.78(s, 1H), 8.48 (t, J=5.8 Hz, 1H), 8.36 (d, J=2.0 Hz, 1H), 8.23 (s, 1H),7.53 (dd, J=8.9, 2.1 Hz, 1H), 7.45 (td, J=7.6, 1.7 Hz, 1H), 7.34 (d,J=8.8 Hz, 1H), 7.26-7.19 (m, 1H), 7.14-7.06 (m, 1H), 5.40 (s, 2H), 4.34(d, J=5.7 Hz, 2H), 3.99 (s, 2H), 3.14-2.99 (m, 1H), 2.41 (s, 3H), 2.19(s, 2H), 1.03 (s, 9H), 1.00-0.87 (m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.63; MS (ES+): 591.6 (M+Na).

Preparation of2-(3-acetyl-5-(2-cyclopropylacetamido)-1H-indol-1-yl)-N-(2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)-N-cyclopropylacetamide(304a)

Reaction of2-(3-acetyl-5-amino-1H-indol-1-yl)-N-(2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)-N-cyclopropylacetamide(286a) (14.36 mg, 0.031 mmol) with 2-cyclopropylacetic acid (4.34 μL,0.046 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column chromatography[silica gel, eluting with hexanes/10% methanol in ethyl acetate (1:0 to1:2)]2-(3-acetyl-5-(2-cyclopropylacetamido)-1H-indol-1-yl)-N-(2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)-N-cyclopropylacetamide(304a) (11 mg, 65%) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 9.80(s, 1H), 8.47 (t, J=5.9 Hz, 1H), 8.36 (d, J=2.0 Hz, 1H), 8.23 (s, 1H),7.55 (dd, J=8.9, 2.1 Hz, 1H), 7.46 (td, J=7.6, 1.7 Hz, 1H), 7.36 (d,J=8.9 Hz, 1H), 7.27-7.19 (m, 1H), 7.14-7.06 (m, 1H), 5.40 (s, 2H), 4.34(d, J=5.8 Hz, 2H), 3.99 (s, 2H), 3.15-3.00 (m, 1H), 2.41 (s, 3H), 2.20(d, J=7.0 Hz, 2H), 1.33-0.81 (m, 5H), 0.55-0.40 (m, 2H), 0.29-0.14 (m,2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.62; MS (ES+): 553.6 (M+1); MS(ES−): 551.4 & 553.6 (M−1).

Preparation of(R)-5-(3-aminopiperidine-1-carboxamido)-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(305a)

To a solution of(R)-5-(3-aminopiperidine-1-carboxamido)-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(299a) (40 mg, 0.067 mmol) in MeOH (15 mL) was added HCl (3N in MeOH)(0.19 mL, 0.57 mmol) and stirred at room temperature overnight. Thereaction mixture was concentrated in vacuum and residue obtained waspurified by flash chromatography [silica (12g), eluting with 0 to 40%DMA-80 in DCM] and preparative HPLC [C₁₈ column, eluting with CH₃CN inwater from 0-100%]. The combined fractions were neutralized with NaHCO₃(sat.) to afford(R)-5-(3-aminopiperidine-1-carboxamido)-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(305a) (40 mg, 93% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ8.57 (s, 1H), 8.50 (t, J=5.9 Hz, 1H), 8.16 (dd, J=2.0, 0.8 Hz, 1H), 7.62(s, 1H), 7.58-7.42 (m, 3H), 7.31 (s, 1H), 7.26-7.18 (m, 1H), 7.17-7.10(m, 1H), 5.60 (s, 2H), 4.33 (d, J=5.7 Hz, 2H), 4.05-3.90 (m, 4H),3.10-2.97 (m, 1H), 2.85-2.69 (m, 1H), 2.67-2.45 (m, 2H), 1.89-1.78 (m,1H), 1.72-1.58 (m, 1H), 1.48-1.32 (m, 1H), 1.25-1.11 (m, 1H), 1.03-0.95(m, 2H), 0.95-0.85 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −73.43 (TFApeak), −121.60; MS (ES+): 599.7 (M+1); (ES−): 597.6 (M−1).

Preparation of1-(2-(cyclopropyl(2-(2-fluoro-3-vinylphenylamino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(306a)

Reaction of1-(2-((2-(3-bromo-2-fluorophenylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(282d) (0.3 g, 0.61 mmol) with Potassium Vinyltrifluoroborate (0.17 g,1.23 mmol) according to the procedure reported in Scheme 78 gave afterworkup and purification by flash column chromatography [silica gel 12 g,eluting with 0 to 20% DMA-80 in DCM]1-(2-(cyclopropyl(2-(2-fluoro-3-vinylphenylamino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(306a) (0.21 g, 78% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ9.86 (s, 1H), 8.18 (d, J=8.1 Hz, 1H), 7.89-7.31 (m, 6H), 7.31-7.21 (m,1H), 7.17-7.06 (m, 1H), 6.84 (dd, J=17.7, 11.2 Hz, 1H), 5.92 (dd,J=17.7, 1.2 Hz, 1H), 5.70 (s, 2H), 5.44 (dd, J=11.2, 1.2 Hz, 1H), 4.21(s, 2H), 3.19-3.05 (m, 1H), 1.07-1.00 (m, 2H), 0.99-0.92 (m, 2H); ¹⁹FNMR (282 MHz, DMSO-d₆) δ −131.22; MS (ES+): 436.5 (M+1), 458.5 (M+Na),MS (ES−): 434.5 (M−1).

Preparation of5-(bis(cyclopropylmethyl)amino)-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(307a)

Reaction of5-amino-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(267e) (0.08 g, 0.17 mmol) with cyclopropanecarbaldehyde (0.036 g, 0.51mmol) according to the procedure reported in Scheme 276 gave afterworkup and purification by flash column chromatography [silica gel (24g), eluting with 0 to 40% DMA-80 in DCM]5-(bis(cyclopropylmethyl)amino)-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(307a) (0.045 g, 46% yield) as white solid; ¹H NMR (300 MHz, DMSO-d₆) δ8.50 (t, J=5.9 Hz, 1H), 7.52 (s, 1H), 7.50-7.40 (m, 3H), 7.27-7.18 (m,2H), 7.18-7.07 (m, 2H), 5.57 (s, 2H), 4.33 (d, J=5.7 Hz, 2H), 3.98 (s,2H), 3.27 (d, J=6.3 Hz, 4H), 3.11-2.98 (m, 1H), 1.15-0.82 (m, 6H),0.54-0.35 (m, 4H), 0.30-0.13 (m, 4H); 19F NMR (282 MHz, DMSO-d₆) δ−121.59; MS (ES+): 581.6 (M+1), MS (ES−): 615.5 (M+Cl).

Preparation of2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-pyrrolo[2,3-c]pyridin-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(308e) Step-1: Preparation of ethyl2-(3-acetyl-5-bromo-1H-pyrrolo[2,3-c]pyridin-1-yl)acetate (308b)

Reaction of 1-(5-bromo-1H-pyrrolo[2,3-c]pyridin-3-yl)ethanone (308a)(1.2 g, 5.02 mmol; Prepared according to the procedure described byHynd, George et al; in PCT Int. Appl., 2014174021, 30 Oct. 2014) withEthyl bromoacetate (1.12 mL, 10.04 mmol), Potassium Carbonate (1.39 g,10.04 mmol) in acetonitrile (40 mL) according to the procedure reportedin step-1 of Scheme 56 gave after workup and purification by flashcolumn chromatography [silica gel 24 g, DMA80 in DCM 0 to 30% aseluents] ethyl 2-(3-acetyl-5-bromo-1H-pyrrolo[2,3-c]pyridin-1-yl)acetate(308b) (0.85 g, 52% yield) as a light orange solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.79 (d, J=1.0 Hz, 1H), 8.58 (s, 1H), 8.18 (d, J=0.9 Hz, 1H),5.36 (s, 2H), 4.19 (q, J=7.1 Hz, 2H), 2.46 (s, 3H), 1.23 (t, J=7.1 Hz,3H); MS (ES+) 325.3, 327.3 (M+1), 347.3, 349.3 (M+Na), MS (ES−) 359.2,361.2 (M+Cl).

Step-2: Preparation of ethyl2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-pyrrolo[2,3-c]pyridin-1-yl)acetate(308c)

Compound 308c was prepared from ethyl2-(3-acetyl-5-bromo-1H-pyrrolo[2,3-c]pyridin-1-yl)acetate (308b) (0.2 g,0.62 mmol) and pyrimidin-5-amine (0.088 g, 0.92 mmol) usingdi-tert-butyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine (0.052 g,0.12 mmol), Potassium Carbonate (0.17 g, 1.23 mmol), Pd₂(dba)₃ (0.056 g,0.062 mmol) according to the procedure reported in step-1 of Scheme 97.This gave after workup and purification by reverse phase chromatography[C18 60 g, acetonitrile in 0.1% TFA in water 0 to 70% as eluents] ethyl2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-pyrrolo[2,3-c]pyridin-1-yl)acetate(308c) (0.02 g, 10% yield) as off-white solid; ¹H NMR (300 MHz, MeOH-d₄)δ 9.12 (s, 2H), 8.59 (s, 1H), 8.50 (d, J=1.1 Hz, 1H), 8.31 (s, 1H), 7.72(d, J=1.1 Hz, 1H), 5.20 (s, 2H), 4.27 (q, J=7.1 Hz, 2H), 2.52 (s, 3H),1.30 (t, J=7.1 Hz, 4H).

Step-3: Preparation 2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-pyrrolo[2,3-c] pyri din-1-yl)acetic acid (308d)

Compound (308d) was prepared from ethyl2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-pyrrolo[2,3-c]pyridin-1-yl)acetate(308c) (0.02 g, 0.059 mmol) using a solution of LiOH (2.82 mg, 0.118mmol) in Water (0.3 mL) and THF (2 mL) according to the procedurereported in Scheme 129 step-2. This gave after workup2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-pyrrolo[2,3-c]pyridin-1-yl)aceticacid (308d) (0.02 g, 0.059 mmol, 100% yield) as a white solid; ¹H NMR(300 MHz, Methanol-d₄) δ 9.06 (s, 2H), 9.01 (s, 1H), 8.86 (s, 1H), 8.76(s, 1H), 8.14 (s, 1H), 5.30 (s, 2H), 2.56 (s, 3H); MS (ES+) 312.3 (M+1),MS (ES−) 310.3 (M−1).

Step-4: Preparation of2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-pyrrolo[2,3-c]pyridin-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(308e)

Reaction of 2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-pyrrolo[2,3-c]pyridin-1-yl)acetic acid (308d) (0.02 g, 0.064 mmol) withN-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide (10b) (0.016g, 0.064 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by column chromatography [silica gel4g, DMA-80 in DCM 0 to 40% as eluents]2-(3-acetyl-5-(pyrimidin-5-ylamino)-1H-pyrrolo [2,3-c]pyridin-1-yl)-N-(2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)-N-cyclopropylacetamide(308e) (0.008 g, 23% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆)δ 9.35 (s, 1H), 9.10 (s, 2H), 8.62 (s, 1H), 8.53 (d, J=1.0 Hz, 1H), 8.48(t, J=5.8 Hz, 1H), 8.41 (s, 1H), 7.68 (d, J=1.0 Hz, 1H), 7.47-7.38 (m,1H), 7.23 (t, J=7.1 Hz, 1H), 7.13-7.04 (m, 1H), 5.50 (s, 2H), 4.35 (d,J=5.7 Hz, 2H), 4.00 (s, 2H), 3.16-3.03 (m, 1H), 2.43 (s, 3H), 1.06-0.95(m, 2H), 0.98-0.86 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.60; MS(ES+): 550.5 (M+1); MS (ES−): 584.5 (M+Cl).

Preparation of2-(3-Acetyl-5-(3-methyl-3-(1-methylpiperidin-4-yl)ureido)-1H-indazol-1-yl)-N-(2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)-N-cyclopropylacetamideHCl salt (309a)

Reaction of3-acetyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (228a) (0.93 g, 1.85 mmol) with diphenyl phosphorazidate (0.41 mL,1.85 mmol), then with N,1-dimethylpiperidin-4-amine (0.29 g, 2.22 mmol)according to the procedure reported in step-3 and step-4 of Scheme 129gave after workup and purification by column chromatography [silica(12g), eluting with DMA80 in DCM from 0 to 40%] and then reverse phasepreparative column chromatography [C18 column, eluting with MeOH inwater (containing 0.1% TFA) from 0 to 100%], followed by conversion toHCl salt using HCl (3 N HCl in MeOH, 10 mL) in methanol (10 mL)2-(3-acetyl-5-(3-methyl-3-(1-methylpiperidin-4-yl)ureido)-1H-indazol-1-yl)-N-(2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)-N-cyclopropylacetamide(309a) (240 mg, 20% yield) HCl salt as a yellow solid; ¹H NMR (300 MHz,DMSO-d₆) δ 10.82 (s, 1H), 8.66-8.49 (m, 2H), 8.27 (t, J=1.3 Hz, 1H),7.60 (d, J=1.4 Hz, 2H), 7.51-7.39 (m, 1H), 7.27-7.19 (m, 1H), 7.18-7.05(m, 1H), 5.71 (s, 2H), 4.42-4.26 (m, 3H), 3.99 (s, 2H), 3.47-3.35 (m,2H), 3.19-3.00 (m, 3H), 2.86 (s, 3H), 2.71 (d, J=4.7 Hz, 3H), 2.59 (s,3H), 2.26-2.04 (m, 2H), 1.83-1.66 (m, 2H), 1.09-0.96 (m, 2H), 0.97-0.83(m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.64; MS (ES+): 626.7 (M+1);(ES−): 624.6 (M−1).

Preparation of(R)-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(3-methyl-3-(1-methylpyrrolidin-3-yl)ureido)-1H-indazole-3-carboxamideHCl salt (310a)

Reaction of3-carbamoyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)-amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (235a) (500 mg, 0.47 mmol) with (R)—N,1-dimethylpyrrolidin-3-amine(98 mg, 0.85 mmol) according to the procedure reported in step-4 ofScheme 129 gave after workup, purification by chromatography [silica(40g), eluting with DMA80 in DCM from 0 to 40%]; followed by [silica (24g), eluting with EtOAc/MeOH (9:1) in hexane from 0 to 90%], thenprep-HPLC [C18 column, 5 injections, eluting with CH₃CN in water(containing 0.1% TFA) from 0-100%]; followed by conversion to HCl saltusing HCl (3 N in MeOH, 10 mL) in methanol (10 mL)(R)-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(3-methyl-3-(1-methylpyrrolidin-3-yl)ureido)-1H-indazole-3-carboxamide(310a) (112 mg, 036% yield) HCl salt as a white solid. ¹H NMR (300 MHz,DMSO-d₆) δ 10.90-10.56 (m, 1H), 8.67-8.49 (m, 2H), 8.20 (t, J=1.4 Hz,1H), 7.71-7.60 (m, 1H), 7.59-7.52 (m, 2H), 7.48-7.40 (m, 1H), 7.37-7.29(m, 1H), 7.28-7.19 (m, 1H), 7.17-7.08 (m, 1H), 5.63 (s, 2H), 5.05-4.89(m, 1H), 4.33 (d, J=5.6 Hz, 2H), 3.98 (s, 2H), 3.69-3.41 (m, 2H),3.31-3.15 (m, 1H), 3.12-2.94 (m, 5H), 2.84 (d, J=4.8 Hz) and 2.78 (d,J=4.9 Hz) (2d, 3H), 2.33-1.96 (m, 2H), 1.07-0.96 (m, 2H), 0.95-0.79 (m,2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.62; MS (ES+): 613.6 (M+1).

Preparation of(S)-5-(3-aminopiperidine-1-carboxamido)-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamideTFA salt (311a)

Reaction of (5)-tert-butyl1-(3-carbamoyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazol-5-ylcarbamoyl)piperidin-3-ylcarbamate(294a) (185 mg, 0.27 mmol) with TFA (0.41 mL, 5.29 mmol) according tothe procedure reported in step-2 of Scheme 2 gave after workup andpurification by column chromatography [silica (12g), eluting with DMA80in DCM from 0 to 40%], then prep-HPLC [C18 column, eluting with CH₃CN inwater (containing 0.1% TFA) from 0-100%] followed by lyophilization(S)-5-(3-aminopiperidine-1-carboxamido)-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(311a) (112 mg, 59% yield) TFA salt as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.73 (s, 1H), 8.52 (t, J=5.8 Hz, 1H), 8.20 (t, J=1.3 Hz, 1H),8.06-7.89 (m, 3H), 7.65 (s, 1H), 7.57-7.51 (m, 2H), 7.46 (td, J=7.6, 1.8Hz, 1H), 7.31 (s, 1H), 7.27-7.19 (m, 1H), 7.18-7.09 (m, 1H), 5.61 (s,2H), 4.33 (d, J=5.7 Hz, 2H), 4.10-4.03 (m, 1H), 3.98 (s, 2H), 3.84-3.72(m, 1H), 3.24-3.12 (m, 2H), 3.11-3.00 (m, 2H), 2.05-1.91 (m, 1H),1.82-1.69 (m, 1H), 1.60-1.43 (m, 2H), 1.04-0.95 (m, 2H), 0.95-0.85 (m,2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −73.79 (TFA peak), −121.60; MS (ES+):599.5 (M+1); (ES−): 597.5 (M−1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-((cyclohexylmethyl)amino)-1H-indazole-3-carboxamide(312a)

Reaction of5-amino-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(267e) (0.1 g, 0.21 mmol) with cyclohexanecarbaldehyde (0.036 g, 0.32mmol) according to the procedure reported in Scheme 276 gave afterworkup and purification by flash column chromatography [silica gel (12g), eluting with 0 to 30% DMA-80 in DCM]1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(cyclohexylmethylamino)-1H-indazole-3-carboxamide(312a) (0.018 g, 15% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆)δ 8.49 (t, J=5.8 Hz, 1H), 7.55-7.40 (m, 2H), 7.34 (d, J=8.9 Hz, 1H),7.29-7.01 (m, 5H), 6.97-6.83 (m, 1H), 5.53 (s, 2H), 4.33 (d, J=5.7 Hz,2H), 3.97 (s, 2H), 3.11-2.96 (m, 1H), 2.88 (d, J=6.5 Hz, 2H), 1.93-1.78(m, 2H), 1.78-1.50 (m, 3H), 1.33-0.80 (m, 10H); ¹⁹F NMR (282 MHz,DMSO-d₆) δ −121.60; MS (ES+): 569.5 (M+1), MS (ES−): 603.5 (M+Cl).

Preparation of1-(2-(cyclopropyl(2-((3-ethyl-2-fluorophenyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(313a)

Compound (313a) was prepared according to the procedure reported inScheme 79 from1-(2-(cyclopropyl(2-(2-fluoro-3-vinylphenylamino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(306a) (0.07 g, 0.161 mmol) in EtOAc (5 mL) using dihydroxypalladium(0.113 mg, 0.804 μmop. This gave after workup and purification by flashchromatography [silica gel 4 g, DMA-80 DCM, 0 to 20% as eluents] toafford1-(2-(cyclopropyl(2-((3-ethyl-2-fluorophenyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(313a) (0.03 g, 43% yield) as a white solid; 1H NMR (300 MHz, DMSO-d₆) δ9.78 (s, 1H), 8.18 (dt, J=8.2, 1.0 Hz, 1H), 7.90-6.91 (m, 8H), 5.70 (s,2H), 4.20 (s, 2H), 3.18-3.04 (m, 1H), 2.61 (q, J=7.4 Hz, 2H), 1.15 (t,J=7.5 Hz, 3H), 1.06-0.95 (m, 2H), 1.00-0.89 (m, 2H); 19F NMR (282 MHz,DMSO-d₆) δ −131.78; MS (ES+): 438.5 (M+1), 460.4 (M+Na), MS (ES−): 472.4(M+Cl).

Preparation of(R)—N-(3-acetyl-1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)(1-hydroxypropan-2-yl)-amino)-2-oxoethyl)-1H-indol-5-yl)-3,3-difluoropiperidine-1-carboxamide(314i) Step-1: Preparation of ethyl2-(3-acetyl-5-amino-1H-indol-1-yl)acetate (314b)

Compound 314b was prepared from ethyl2-(3-acetyl-5-nitro-1H-indol-1-yl)acetate (314a) (6.00 g, 20.67 mmol,prepared according to procedure reported by Venkatanarayana, Muvvala andDubey, Pramod K. in Letters in Organic Chemistry, 9(3), 192-197; 2012)using ammonium chloride (17.69 g, 331 mmol), zinc powder (10.82 g, 165mmol) in THF (120 mL), methanol (30 mL); according to the procedurereported in step-4 of Scheme 267. This gave after workup andpurification by flash column chromatography [Silica gel 120 g, elutingwith ethyl acetate/methanol (9:1) in hexanes from 0-100%] ethyl2-(3-acetyl-5-amino-1H-indol-1-yl)acetate (314b) (4.28 g, 80% yield) asa yellow solid; ¹H NMR (300 MHz, DMSO-d₆) δ 8.08 (s, 1H), 7.41 (d, J=2.2Hz, 1H), 7.12 (d, J=8.7 Hz, 1H), 6.57 (dd, J=8.6, 2.2 Hz, 1H), 5.09 (s,2H), 4.89 (s, 2H, D₂O exchangeable), 4.16 (q, J=7.0 Hz, 2H), 2.36 (s,3H), 1.22 (t, J=7.1 Hz, 3H); MS (ES+): 261.4 (M+1).

Step-2: Preparation of ethyl2-(3-acetyl-5-(phenoxycarbonylamino)-1H-indol-1-yl)acetate (314c)

To a biphasic solution of ethyl2-(3-acetyl-5-amino-1H-indol-1-yl)acetate (314b) (1.00 g, 3.84 mmol) inEtOAc (10 mL) and sat. NaHCO₃ (5 mL) was added phenyl chloroformate(0.627 mL, 4.99 mmol) and stirred at room temperature for 13 h. Theorganic layer was separated and aqueous layer was extracted with EtOAc(2×50 mL). The combined organics were washed with brine, dried,filtered, and concentrated in vacuum to afford ethyl2-(3-acetyl-5-(phenoxycarbonylamino)-1H-indol-1-yl)acetate (314c) (1.41g, 96% yield) as a brown solid; ¹H NMR (300 MHz, DMSO-d₆) δ 10.16 (s,1H), 8.31 (s, 1H), 7.47-7.40 (m, 3H), 7.27-7.21 (m, 3H), 7.19-7.12 (m,1H), 6.87-6.66 (m, 1H), 5.21 (s, 2H), 4.18 (q, J=7.1 Hz, 2H), 2.42 (s,3H), 1.23 (t, J=7.1 Hz, 3H); MS (ES+): 381.4 (M+1).

Step-3: Preparation of ethyl2-(3-acetyl-5-(3,3-difluoropiperidine-1-carboxamido)-1H-indol-1-yl)acetate(314d)

To a solution of ethyl2-(3-acetyl-5-(phenoxycarbonylamino)-1H-indol-1-yl)acetate (314c) (1.39g, 3.65 mmol) in THF (40 mL) was added 3,3-difluoropiperidinehydrochloride (0.576 g, 3.65 mmol), a solution of sodium bicarbonate(1.535 g, 18.27 mmol) in water (5 mL) and stirred at 65° C. for 4.5 h.The reaction mixture was cooled to room temperature and partitionedbetween water (100 mL) and EtOAc (100 mL). The aqueous layer wasseparated, extracted with EtOAc (100 mL). The combined organics werewashed with brine, dried, filtered and evaporated to dryness. The crudeproduct was purified by flash column chromatography [Silica gel, 24 geluting with ethyl acetate/methanol (9:1) in hexanes from 0-100%] toafford ethyl2-(3-acetyl-5-(3,3-difluoropiperidine-1-carboxamido)-1H-indol-1-yl)acetate(314d) (0.991 g, 67% yield) as a yellow solid; ¹H NMR (300 MHz, DMSO-d₆)δ 8.66 (s, 1H), 8.26 (s, 1H), 8.19 (dd, J=2.0, 0.7 Hz, 1H), 7.47-7.32(m, 2H), 5.19 (s, 2H), 4.17 (q, J=7.1 Hz, 2H), 3.80 (t, J=12.1 Hz, 2H),3.51 (t, J=5.5 Hz, 2H), 2.42 (s, 3H), 2.15-1.96 (m, 2H), 1.79-1.64 (m,2H), 1.22 (t, J=7.1 Hz, 3H); MS (ES+): 408.5 (M+1), 815.8 (2M+1), 834.8(2M+Na); MS (ES−): 406.4 (M−1).

Step-4: Preparation of2-(3-Acetyl-5-(3,3-difluoropiperidine-1-carboxamido)-1H-indol-1-yl)aceticacid (314e)

Compound (314e) was prepared from ethyl2-(3-acetyl-5-(3,3-difluoropiperidine-1-carboxamido)-1H-indol-1-yl)acetate(314d) (0.956 g, 2.347 mmol) using a solution of LiOH (0.169 g, 7.04mmol) in Water (3 mL) and THF (15 mL) according to the procedurereported in Scheme 129 step-2. This gave after workup2-(3-acetyl-5-(3,3-difluoropiperidine-1-carboxamido)-1H-indol-1-yl)aceticacid (314e) (0.557 g, 63% yield) as a brick-red solid; ¹H NMR (300 MHz,DMSO-d₆) δ 13.22 (s, 1H), 8.66 (s, 1H), 8.26 (s, 1H), 8.22-8.13 (m, 1H),7.50-7.28 (m, 2H), 5.07 (s, 2H), 3.80 (t, J=12.1 Hz, 2H), 3.51 (t, J=5.4Hz, 2H), 2.41 (s, 3H), 2.17-1.92 (m, 2H), 1.71 (s, 2H); MS (ES−): 378.3(M−1), 757.5 (2M−1).

Step-5: Preparation of(R)-2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)-amino)-N-(2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)acetamide(314g)

Compound 314f was prepared according to the procedure reported in step-2of Scheme 35 from2-chloro-N-(2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)acetamide (115b)(2.00 g, 6.71 mmol) and(R)-1-((tert-butyldimethylsilyl)oxy)propan-2-amine (314f) (1.65 g, 8.72mmol, prepared according to the procedure reported by Chen, Yi et al, inU S. Pat. Appl. Publ., 20040204427, 14 Oct. 2004). This gave afterworkup and purification by flash column chromatography [Silica gel, 40 geluting with ethyl acetate in hexanes from 0-20%](R)-2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)-amino)-N-(2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)acetamide(314g) (1.64 g, 54% yield) as a thick colorless oil; ¹H NMR (300 MHz,DMSO-d₆) δ 9.99 (s, 1H), 8.22 (td, J=7.9, 1.7 Hz, 1H), 7.64-7.56 (m,1H), 7.52-7.37 (m, 3H), 7.26 (td, J=7.9, 1.0 Hz, 1H), 7.10-7.03 (m, 1H),3.45 (d, J=5.6 Hz, 2H), 3.37 (d, J=1.6 Hz, 2H), 3.16 (d, J=5.2 Hz, 1H),2.77-2.61 (m, 1H), 0.95 (d, J=6.3 Hz, 3H), 0.83 (s, 9H), 0.00 (s, 3H),−0.00 (s, 3H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −130.68; MS (ES+): 451.5,453.5 (M+1); MS (ES−): 449.4, 451.4 (M−1).

Step-6: Preparation of(R)—N-(3-acetyl-1-(2-((1-(tert-butyldimethylsilyloxy)propan-2-yl)(2-(2′-chloro-2-fluorobiphenyl-3-ylamino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indol-5-yl)-3,3-difluoropiperidine-1-carboxamide(314h)

Compound 314h was prepared from(R)-2-(1-(tert-butyldimethylsilyloxy)propan-2-ylamino)-N-(2′-chloro-2-fluorobiphenyl-3-yl)acetamide(314g) (297 mg, 0.66 mmol) by reaction with2-(3-Acetyl-5-(3,3-difluoropiperidine-1-carboxamido)-1H-indol-1-yl)aceticacid (314e) (250 mg, 0.766 mmol) according to the procedure reported instep-3 of Scheme 2. This gave after workup and purification by flashcolumn chromatography [Silica gel, 12 g eluting with methanol in DCMfrom 0-10%](R)—N-(3-acetyl-1-(2-((1-(tert-butyldimethylsilyloxy)propan-2-yl)(2-(2′-chloro-2-fluorobiphenyl-3-ylamino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indol-5-yl)-3,3-difluoropiperidine-1-carboxamide(314h) (0.27 g, 51% yield) as a yellow solid; MS (ES+): 812.6 (M+1); MS(ES−): 846.6 (M+Cl).

Step-7: Preparation of(R)—N-(3-acetyl-1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indol-5-yl)-3,3-difluoropiperidine-1-carboxamide(314i)

Compound 314i was prepared from(R)—N-(3-acetyl-1-(2-((1-(tert-butyldimethylsilyloxy)propan-2-yl)(2-(2′-chloro-2-fluorobiphenyl-3-ylamino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indol-5-yl)-3,3-difluoropiperidine-1-carboxamide(314h) (204 mg, 0.25 mmol) by reaction with 12N aq. HCl (0.209 mL, 2.51mmol) in MTBE (5.00 mL) according to the procedure reported in step-3 ofScheme 292. This gave after workup and purification by flash columnchromatography [Silica gel, 24 g eluting with methanol in DCM from0-20%)(R)—N-(3-acetyl-1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indol-5-yl)-3,3-difluoropiperidine-1-carboxamide(314i) (50 mg, 29% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ10.27 & 9.97 (2s, 1H, D₂O exchangeable), 8.635 & 8.645 (s, 1H),8.29-7.84 (m, 4H), 7.66-7.57 (m, 1H), 7.55-7.26 (m, 4H), 7.27-7.02 (m,2H), 5.48 (t, J=5.7 Hz) & 4.88-4.81 (m, (1H), 5.36 & 5.17 (2s, 2H),4.59-4.43 (m, 1H), 4.28-4.13 (m, 1H), 4.00 & 3.94 (2s, 1H), 3.80 (t,J=12.1 Hz, 2H), 3.58-3.48 (m, 4H), 2.41 (s, 1H), 2.38 (s, 2H), 2.17-1.94(m, 2H), 1.81-1.59 (m, 2H), 1.19 (d, J=6.6 Hz) & 1.05 (d, J=6.9 Hz) (2d,3H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −101.10, −127.32; MS (ES+): 720.5(M+Na); MS (ES−): 696.6 (M−1).

Preparation of1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(2-(1-methylpiperidin-4-yl)acetamido)-1H-indazole-3-carboxamide(315a)

Reaction of5-amino-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(267e) (0.15 g, 0.317 mmol) with 2-(1-methylpiperidin-4-yl)acetic acid(0.055 g, 0.349 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup and purification by flash columnchromatography [silica gel 12 g, DMA80 in DCM 0 to 100% as eluents]1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(2-(1-methylpiperidin-4-yl)acetamido)-1H-indazole-3-carboxamide(315a) (0.053 g, 27% yield) as an off-white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 9.99 (s, 1H), 8.49 (t, J=5.8 Hz, 1H), 8.46-8.43 (m, 1H), 7.66(s, 1H), 7.64-7.52 (m, 2H), 7.50-7.41 (m, 1H), 7.35 (s, 1H), 7.23 (t,J=6.9 Hz, 1H), 7.16-7.07 (m, 1H), 5.62 (s, 2H), 4.33 (d, J=5.7 Hz, 2H),3.98 (s, 2H), 3.13-2.99 (m, 1H), 2.84-2.73 (m, 2H), 2.24 (d, J=7.0 Hz,2H), 2.18 (s, 3H), 2.02-1.82 (m, 2H), 1.81-1.58 (m, 3H), 1.35-1.17 (m,2H), 1.03-0.95 (m, 2H), 0.95-0.85 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.59; MS (ES+): 612.6 (M+1), MS (ES−): 646.5 (M+Cl).

Preparation of1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(pyrimidin-5-ylamino)-1H-indazole-3-carboxamide(316f) Step-1: Preparation of tert-butyl2-(5-bromo-3-cyano-1H-indazol-1-yl)acetate (316b)

Reaction of 5-bromo-1H-indazole-3-carbonitrile (316a) (0.85 g, 3.83mmol, prepared according to the procedure reported By Boyd, Scott et al;in Journal of Medicinal Chemistry, 58(8), 3611-3625; 2015) withtert-butylbromoacetate (1.13 mL, 7.66 mmol) in acetonitrile (40 mL)using potassium carbonate (1.06 g, 7.66 mmol) as base, according to theprocedure reported in step-1 of Scheme 43 gave after workup andpurification by column chromatography [silica gel (24 g), eluting withEtOAc in hexane 0 to 60%] tert-butyl2-(5-bromo-3-cyano-1H-indazol-1-yl)acetate (316b) (0.95 g, 74% yield) asan off-white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 8.21 (dd, J=1.8, 0.7 Hz,1H), 7.94-7.88 (m, 1H), 7.76 (dd, J=9.0, 1.8 Hz, 1H), 5.53 (s, 2H), 1.40(s, 9H).

Step-2: Preparation of tert-butyl2-(3-cyano-5-(pyrimidin-5-ylamino)-1H-indazol-1-yl)acetate (316c)

Reaction of tert-butyl 2-(5-bromo-3-cyano-1H-indazol-1-yl)acetate (316b)(0.5 g, 1.49 mmol), with pyrimidin-5-amine (212 mg, 2.23 mmol) usingPotassium carbonate (0.41 g, 2.97 mmol),di-tert-butyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine (95 mg, 0.223mmol), Pd₂(dba)₃ (95 mg, 0.104 mmol) according to the procedure reportedin step-1 of Scheme 97 gave after workup and purification by flashcolumn chromatography [silica gel (12 g), eluting with EtOAc in Hexane 0to 100%] tert-butyl2-(3-cyano-5-(pyrimidin-5-ylamino)-1H-indazol-1-yl)acetate (316c) (0.375g, 72% yield) as an off-white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 8.78(s, 1H), 8.70 (s, 1H), 8.64 (s, 2H), 7.84 (dd, J=9.1, 0.7 Hz, 1H), 7.49(dd, J=2.1, 0.7 Hz, 1H), 7.42 (dd, J=9.1, 2.1 Hz, 1H), 5.46 (s, 2H),1.42 (s, 9H); MS (ES+): 351.4 (M+1), MS (ES−): 349.3 (M−1).

Step-3: Preparation of tert-butyl2-(3-carbamoyl-5-(pyrimidin-5-ylamino)-1H-indazol-1-yl)acetate (316d)

Reaction of tert-butyl2-(3-cyano-5-(pyrimidin-5-ylamino)-1H-indazol-1-yl)acetate (316c) (350mg, 1.0 mmol) in EtOH (10 mL) with conc. NH₄OH Ammonium hydroxide (0.78mL, 19.98 mmol) and Hydrogen peroxide (35% aqueous, 0.46 mL, 14.98 mmol)according to the procedure reported in Scheme 65 gave after workuptert-butyl2-(3-carbamoyl-5-(pyrimidin-5-ylamino)-1H-indazol-1-yl)acetate (316d)(0.32 g, 87% yield) as a off-white solid; ¹H NMR (300 MHz, DMSO-d₆) δ8.64 (s, 1H), 8.63 (s, 1H), 8.52 (s, 2H), 7.94-7.89 (m, 1H), 7.73-7.66(m, 2H), 7.39 (s, 1H), 7.33 (dd, J=9.0, 2.2 Hz, 1H), 5.32 (s, 2H), 1.42(s, 9H); MS (ES−): 403.3 (M−1).

Step-4: Preparation of2-(3-carbamoyl-5-(pyrimidin-5-ylamino)-1H-indazol-1-yl)acetic acid(316e)

Reaction of tert-butyl2-(3-carbamoyl-5-(pyrimidin-5-ylamino)-1H-indazol-1-yl)acetate (316d)(320 mg, 0.87 mmol) with TFA (1.00 mL, 13.03 mmol) according to theprocedure reported in step-2 of Scheme 2 gave after workup andtrituration of crude with toluene (2×15 mL) and 30% EtOAc-hexane (10mL), 2-(3-carbamoyl-5-(pyrimidin-5-ylamino)-1H-indazol-1-yl)acetic acid(316e) (0.31 g, 84% yield) as a dark brown solid; MS (ES+): 313.3 (M+1).

Step-5: Preparation of1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(pyrimidin-5-ylamino)-1H-indazole-3-carboxamide(316f)

Reaction of2-(3-carbamoyl-5-(pyrimidin-5-ylamino)-1H-indazol-1-yl)acetic acid(316e) (94 mg, 0.30 mmol) withN-(2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-2-(cyclopropylamino)acetamide(255a) (60 mg, 0.19 mmol) according to the procedure reported in step-3of Scheme 2 gave after workup and purification by flash column [silicagel (12 g), eluting with CMA-80 in CHCl₃ 0-50%]1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(pyrimidin-5-ylamino)-1H-indazole-3-carboxamide(316f) (0.018 g, 16% yield) as an off-white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 9.96 (s, 1H), 8.62 (d, J=1.6 Hz, 2H), 8.52 (s, 2H), 7.98 (t,J=7.9 Hz, 1H), 7.92 (d, J=2.1 Hz, 1H), 7.75-7.54 (m, 3H), 7.52-7.19 (m,6H), 7.13-7.03 (m, 1H), 5.68 (s, 2H), 4.24 (s, 2H), 3.19-3.05 (m, 1H),1.09-0.99 (m, 2H), 1.00-0.90 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−126.71; MS (ES+) 613.5 (M+1), MS (ES−): 647.5 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(pyrimidin-5-ylamino)-1H-indazole-3-carboxamide(317a)

Reaction of2-(3-carbamoyl-5-(pyrimidin-5-ylamino)-1H-indazol-1-yl)acetic acid(316e) (87 mg, 0.28 mmol) withN-(3-chloro-2-fluorobenzyl)-2-(isopropylamino)acetamide (19c) (60 mg,0.23 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column [silica gel (4 g),eluting with DMA-80 in DCM 0-40%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(pyrimidin-5-ylamino)-1H-indazole-3-carboxamide(317a) (0.015 g, 12% yield) as an off-white solid; ¹H NMR (300 MHz,DMSO-d₆) (a mixture of two rotamers) δ 8.83 and 8.37 (2t, J=5.7 Hz, 1H),8.62 and 8.61 (2s, 1H), 8.52 (s, 2H), 7.929 and 7.92 (2s, 1H), 7.73-7.01(m, 8H), 5.57 and 5.43 (2s, 2H), 4.63-4.50 and 4.32-4.20 (2m, 1H), 4.46and 4.32 (2d, J=5.8 Hz, 2H), 4.18 and 3.84 (2s, 2H), 1.22 and 0.99 (2d,J=6.8 Hz, 6H); ¹⁹F NMR (282 MHz, DMSO-d₆) (a mixture of two rotamers) δ−121.21, −121.72; MS (ES+): 553.5 (M+1), MS (ES−): 587.4 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(3-cyanocyclobutyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(318b) Step-1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-((3-cyanocyclobutyl)amino)acetamide (318a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (410 mg,1.74 mmol) with 3-aminocyclobutanecarbonitrile (250 mg, 2.61 mmol)according to the procedure reported in step-2 of Scheme 35 gave afterworkup N-(3-chloro-2-fluorobenzyl)-2-((3-cyanocyclobutyl)amino)acetamide(318a) (0.514 g, 100% yield) as a yellow wax; MS (ES+): 296.3 (M+1); MS(ES−): 294.3 (M−1).

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(3-cyanocyclobutyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(318b)

Reaction ofN-(3-chloro-2-fluorobenzyl)-2-((3-cyanocyclobutyl)amino)acetamide (318a)(514 mg, 1.74 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e)(381 mg, 1.74 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup and purification by flash columnchromatography [Silica gel, (24 g) eluting with ethyl acetate/methanol(9:1) in hexanes from 0-100%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(3-cyanocyclobutyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(318b) (0.257 g, 30% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆)δ 8.91 (t, J=5.8 Hz) & 8.50 (t, J=5.8 Hz) (t, 1H), 8.19 & 8.16 (2s, 1H),7.71 (bs, 1H), 7.62-7.36 (m, 4H), 7.33-7.04 (m, 3H), 5.57 & 5.41 (2s,2H), 4.71-4.06 (m, 5H), 3.13-2.90 (m, 1H), 2.74-2.53 (m, 2H), 2.46-2.30(m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.23, −121.59; MS (ES+): 519.4(M+Na); MS (ES−): 495.4 (M−1).

Preparation of1-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(pyrimidin-5-ylamino)-1H-indazole-3-carboxamide(319a)

Reaction of2-(3-carbamoyl-5-(pyrimidin-5-ylamino)-1H-indazol-1-yl)acetic acid(316e) (96 mg, 0.31 mmol) withN-(6-bromopyridin-2-yl)-2-(isopropylamino)acetamide (28b) (60 mg, 0.22mmol) according to the procedure reported in step-3 of Scheme 2 gaveafter workup and purification by flash column [silica gel (4 g), elutingwith DMA-80 in DCM 0-50%]1-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(pyrimidin-5-ylamino)-1H-indazole-3-carboxamide(319a) (0.014 g, 11% yield) as an off-white solid; ¹H NMR (300 MHz,DMSO-d₆) (a mixture of two rotamers) δ 11.20 and 10.82 (2s, 1H),8.64-8.60 (m, 2H), 8.52 and 8.51 (2s, 2H), 8.16 and 8.01 (2d, J=8.2 Hz,1H), 7.92 and 7.90 (2d, J=2.1 Hz, 1H), 7.87-7.53 (m, 3H), 7.46-7.23 (m,3H), 5.61 and 5.44 (2s, 2H), 4.69-4.55 and 4.38-4.26 (2m, 1H), 4.43 and4.03 (2s, 2H), 1.24 and 1.03 (2d, J=6.8 Hz, 6H); MS (ES+): 566.4, 568.4(M+1), MS (ES−): 600.3, 602.3 (M+Cl).

Preparation of1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(3-methyl-3-(1-methylpiperidin-4-yl)ureido)-1H-indazole-3-carboxamide(320a)

Compound 320a was prepared from3-carbamoyl-1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (230b) (200 mg, 0.353 mmol) according to the procedure reported instep-3 of scheme-223. This gave after work up and purification by flashcolumn chromatography [silica gel (4 g), eluting with DMA80 in DCM 0 to100%]1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(3-methyl-3-(1-methylpiperidin-4-yl)ureido)-1H-indazole-3-carboxamide(320a) (0.023 g, 9% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆)(a mixture of two rotamers) δ 10.25 and 9.77 (2s, 1H), 8.417 and 8.41(2s, 1H), 8.175 and 8.17 (2s, 1H), 8.09 and 7.95 (t, J=7.8 Hz, 1H),7.70-7.53 (m, 2H), 7.51-7.36 (m, 3H), 7.36-6.90 (m, 5H), 5.57 and 5.44(2s, 2H), 4.71-4.55 and 4.39-4.25 (2m, 1H), 4.46 (s, 1H) and 4.18-4.01(m, 2H), 3.06-2.90 (m, 2H), 2.83 and 2.83 (2s, 3H), 2.40-2.14 (m, 5H),1.87-1.68 (m, 2H), 1.64-1.51 (m, 2H), 1.25 and 1.06 (2d, J=6.7 Hz, 6H);¹⁹F NMR (282 MHz, DMSO-d₆) (a mixture of two rotamers) δ −126.78,−126.98; MS (ES+): 691.5 (M+1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(1-methylpiperidine-4-carboxamido)-1H-indazole-3-carboxamide(321a)

Reaction of5-amino-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(267e) (170 mg, 0.36 mmol) with 1-methylpiperidine-4-carboxylic acid (62mg, 0.43 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column chromatography[silica (12g), eluting with DMA80 in DCM from 0 to 70%], followed byconversion of freebase to HCl salt using HCl (3N in MeOH, 3 mL) in MeOH(10 mL)1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(1-methylpiperidine-4-carboxamido)-1H-indazole-3-carboxamide(321a) (85 mg, 37% yield) HCl salt as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 10.22 (s, 1H), 9.75 (brs, 1H), 8.53 (t, J=5.8 Hz, 1H),8.49-8.42 (m, 1H), 7.68 (s, 1H), 7.63-7.57 (m, 2H), 7.49-7.42 (m, 1H),7.35 (s, 1H), 7.27-7.19 (m, 1H), 7.15-7.08 (m, 1H), 5.63 (s, 2H), 4.33(d, J=5.7 Hz, 2H), 3.98 (s, 2H), 3.52-3.44 (m, 2H), 3.13-2.91 (m, 3H),2.84-2.70 (m, 4H), 2.09-1.99 (m, 2H), 1.98-1.82 (m, 2H), 1.02-0.96 (m,2H), 0.95-0.87 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.58; MS (ES+):598.6 (M+1); (ES−): 632.5 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-6-(3,3-dimethylbutanamido)-1H-indazole-3-carboxamide(322b) Step-1: Preparation of6-amino-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(322a)

Reaction of tert-butyl(3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazol-6-yl)carbamate(273a) (15 mg, 0.026 mmol) with 2,2,2-trifluoroacetic acid (0.121 mL,1.57 mmol) according to the procedure reported in step-2 of Scheme-2gave after workup and purification by flash column chromatography[silica gel, eluting with hexanes/10% methanol in ethyl acetate (1:0 to0:1)]6-amino-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(322a) (8 mg, 65%) as a light pink solid; ¹H NMR (300 MHz, Methanol-d₄)δ 7.88 (d, J=8.7 Hz, 1H), 7.38-7.28 (m, 1H), 7.27-7.20 (m, 1H),7.07-6.99 (m, 1H), 6.73 (dd, J=8.7, 1.8 Hz, 1H), 6.62-6.59 (m, 1H), 5.49(s, 2H), 4.44 (s, 2H), 4.13 (s, 2H), 3.12-2.98 (m, 1H), 1.09-0.94 (m,4H); MS (ES+): 495.3 & 497.2 (M+Na).

Step-2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-6-(3,3-dimethylbutanamido)-1H-indazole-3-carboxamide(322b)

Reaction of6-amino-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(322a) (26.5 mg, 0.056 mmol) with 3,3-dimethylbutanoic acid (10.92 μL,0.084 mmol) according to the procedure reported in step-3 of Scheme-2gave after workup and purification by flash column chromatography[silica gel, eluting with hexanes/10% methanol in ethyl acetate (1:0 to1:1)]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-6-(3,3-dimethylbutanamido)-1H-indazole-3-carboxamide(322b) (11 mg, 34% yield) as an off-white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 10.03 (s, 1H), 8.52 (t, J=5.7 Hz, 1H), 8.09-7.99 (m, 2H),7.70 (s, 1H), 7.49-7.40 (m, 1H), 7.35 (s, 1H), 7.30-7.18 (m, 2H), 7.12(t, J=7.8 Hz, 1H), 5.59 (s, 2H), 4.32 (d, J=5.8 Hz, 2H), 3.99 (s, 2H),3.14-2.97 (m, 1H), 2.22 (s, 2H), 1.03 (s, 9H), 1.08-0.87 (m, 4H); ¹⁹FNMR (282 MHz, DMSO-d₆) δ −121.63; MS (ES+): 571.5 (M+1), 593.5 & 595.5(M+Na); MS (ES−): 569.4 & 571.4 (M−1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-6-(2-cyclopropylacetamido)-1H-indazole-3-carboxamide(323a)

Reaction of6-amino-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(322a) (26.5 mg, 0.056 mmol) with 2-cyclopropylacetic acid (7.98 μL,0.084 mmol) according to the procedure reported in step-3 of Scheme-2gave after workup and purification by flash column chromatography[silica gel, eluting with hexanes/10% methanol in ethyl acetate (1:0 to1:2)]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-6-(2-cyclopropylacetamido)-1H-indazole-3-carboxamide(323a) (14 mg, 45% yield) as a light brown solid; ¹H NMR (300 MHz,DMSO-d₆) δ 10.07 (s, 1H), 8.52 (t, J=5.9 Hz, 1H), 8.13-7.96 (m, 2H),7.70 (s, 1H), 7.53-7.40 (m, 1H), 7.35 (s, 1H), 7.29-7.18 (m, 2H), 7.13(t, J=7.9 Hz, 1H), 5.59 (s, 2H), 4.33 (d, J=5.7 Hz, 2H), 3.99 (s, 2H),3.12-2.92 (m, 1H), 2.23 (d, J=7.0 Hz, 2H), 1.14-0.78 (m, 5H), 0.56-0.35(m, 2H), 0.29-0.10 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.63; MS(ES+): 555.5 (M+1), 577.5 & 579.5 (M+Na); MS (ES−): 589.5 & 591.4(M+Cl).

Preparation of2-(3-acetyl-5-(2-aminoacetamido)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(324b) Step-1: Preparation of tert-butyl(2-((3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indol-5-yl)-amino)-2-oxoethyl)carbamate(324a)

Reaction of2-(3-acetyl-5-amino-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(286a) (54 mg, 0.12 mmol) with 2-(tert-butoxycarbonylamino)acetic acid(30.7 mg, 0.172 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup and purification by flash columnchromatography [silica gel, eluting with hexanes/10% methanol in ethylacetate (1:0 to 0:1)] tert-butyl(2-((3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indol-5-yl)-amino)-2-oxoethyl)carbamate(324a) (63 mg, 87% yield) as a light brown solid; ¹H NMR (300 MHz,DMSO-d₆) δ 9.90 (s, 1H), 8.50-8.34 (m, 2H), 8.25 (s, 1H), 7.56-7.34 (m,3H), 7.27-6.99 (m, 3H), 5.41 (s, 2H), 4.35 (d, J=5.9 Hz, 2H), 3.99 (s,2H), 3.73 (d, J=6.0 Hz, 2H), 3.15-3.01 (m, 1H), 2.41 (s, 3H), 1.40 (s,9H), 1.04-0.86 (m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.63; MS (ES−):626.5 & 628.5 (M−1).

Step-2: Preparation of2-(3-acetyl-5-(2-aminoacetamido)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(324b)

Reaction of tert-butyl(2-((3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indol-5-yl)-amino)-2-oxoethyl)carbamate(324a) (55 mg, 0.088 mmol) with 2,2,2-trifluoroacetic acid (0.10 mL,1.31 mmol) according to the procedure reported in step-2 of Scheme 2gave after workup and purification by flash column chromatography[silica gel, eluting with dichloromethane/DMA80 (1:0 to 2:1)]2-(3-acetyl-5-(2-aminoacetamido)-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(324b) (37 mg, 80%) as an off-white solid; ¹H NMR (300 MHz, DMSO-d₆) δ9.83 (s, 1H), 8.47 (t, J=5.8 Hz, 1H), 8.41 (d, J=2.0 Hz, 1H), 8.24 (s,1H), 7.53 (dd, J=8.8, 2.1 Hz, 1H), 7.46 (td, J=7.6, 1.7 Hz, 1H), 7.37(d, J=8.8 Hz, 1H), 7.27-7.20 (m, 1H), 7.16-7.07 (m, 1H), 5.41 (s, 2H),4.35 (d, J=5.7 Hz, 2H), 3.99 (s, 2H), 3.27 (s, 2H), 3.13-2.99 (m, 1H),2.41 (s, 3H), 2.07 (bs, 2H), 1.08-0.78 (m, 4H); ¹⁹F NMR (282 MHz,DMSO-d₆) δ −121.62; MS (ES+): 528.5 & 530.5 (M+1).

Preparation ofN-(3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indol-5-yl)-3-aminobenzamide(325b) Step-1: Preparation of tert-butyl(3-((3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indol-5-yl)carbamoyl)phenyl)carbamate(325a)

Reaction of2-(3-acetyl-5-amino-1H-indol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(286a) (54 mg, 0.12 mmol) with 3-(tert-butoxycarbonylamino)benzoic acid(40.8 mg, 0.172 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup tert-butyl(3-((3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indol-5-yl)carbamoyl)phenyl)carbamate(325a) which was used as such for next step. MS (ES+): 690.6 (M+1);712.5 (M+Na).

Step-2: Preparation ofN-(3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indol-5-yl)-3-aminobenzamide(325b)

Reaction of tert-butyl(3-((3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indol-5-yl)carbamoyl)phenyl)carbamate(325a) (crude from step-1) with 2,2,2-trifluoroacetic acid (0.13 mL,1.73 mmol) according to the procedure reported in step-2 of Scheme 2gave after workup and purification by flash column chromatography[silica gel, eluting with dichloromethane/DMA80 (1:0 to 2:1)]N-(3-acetyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indol-5-yl)-3-aminobenzamide(325b) (19 mg, 28% for 2 steps) as a light brown solid; ¹H NMR (300 MHz,DMSO-d₆) δ 10.07 (s, 1H), 8.55 (d, J=2.1 Hz, 1H), 8.47 (t, J=5.8 Hz,1H), 8.25 (s, 1H), 7.62 (dd, J=8.9, 2.1 Hz, 1H), 7.46 (td, J=7.6, 1.7Hz, 1H), 7.39 (d, J=8.9 Hz, 1H), 7.29-7.20 (m, 1H), 7.18-7.08 (m, 4H),6.73 (dt, J=7.0, 2.3 Hz, 1H), 5.42 (s, 2H), 5.30 (s, 2H), 4.35 (d, J=5.7Hz, 2H), 4.00 (s, 2H), 3.13-3.01 (m, 1H), 2.43 (d, J=2.2 Hz, 3H),1.04-0.87 (m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.62; MS (ES+): 590.5& 592.5 (M+1); MS (ES−): 624.5 & 626.4 (M+Cl).

Preparation of5-amino-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-pyrazolo[3,4-b]pyridine-3-carboxamide(326b) Step-1: Preparation oftert-butyl(3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-pyrazolo[3,4-b]pyridin-5-yl)carbamate(326a)

Compound 326a was prepared from3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-pyrazolo[3,4-b]pyridine-5-carbonylazide (291g) (0.183 mmol) and 2-methylpropan-2-ol (0.105 mL, 1.1 mmol)using TEA (0.051 mL, 0.37 mmol) as base according to the procedurereported in step-4 of Scheme 129 to afford after workup and purificationby column chromatography [silica gel, eluting with DCM in methanol (1:0to 19:1)] tert-butyl(3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-pyrazolo[3,4-b]pyridin-5-yl)carbamate(326a) (12 mg, 11% yield for two steps) as a white solid; MS (ES+):574.6 (M+1); 596.6 (M+Na).

Step-2: Preparation of5-amino-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-pyrazolo[3,4-b]pyridine-3-carboxamide(326b)

Compound 326b was prepared from tert-butyl(3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-pyrazolo[3,4-b]pyridin-5-yl)carbamate(326a) (12 mg, 0.02 mmol), according to the procedure reported in step-2of Scheme 2. This gave after workup and purification by columnchromatography [silica gel, eluting with DCM in DMA-80 (1:0 to 2:1)]5-amino-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-pyrazolo[3,4-b]pyridine-3-carboxamide(326b) (6 mg, 61%); ¹H NMR (300 MHz, DMSO-d₆) δ 8.50 (t, J=5.6 Hz, 1H),8.07 (d, J=2.6 Hz, 1H), 7.64 (s, 1H), 7.61 (d, J=2.6 Hz, 1H), 7.52-7.41(m, 1H), 7.30 (s, 1H), 7.26-7.19 (m, 1H), 7.19-7.09 (m, 1H), 5.55 (s,2H), 5.35 (s, 2H), 4.32 (d, J=5.7 Hz, 2H), 3.97 (s, 2H), 3.12-2.92 (m,1H), 1.01-0.81 (m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.59; MS (ES+):474.4 & 476.4 (M+1); MS (ES−): 508.3 & 510.3 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(piperidine-1-carbonyl)-1H-indazole-3-carboxamide(327a)

Reaction of3-carbamoyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-1H-indazole-5-carbonylazide (145a) (200 mg, 0.378 mmol) in toluene (20 mL) with piperidine(0.064 g, 0.756 mmol) using TEA (0.153 g, 1.42 mmol) as base accordingto the procedure reported in step-4 of Scheme 129 gave after workup1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(isopropyl)amino)-2-oxoethyl)-5-(piperidine-1-carbonyl)-1H-indazole-3-carboxamide (327a)

(70 mg, 33% yield) as an off-white solid; ¹H NMR (300 MHz, DMSO-d₆); δ8.89-8.82 (m, 1H). 8.17 (s, 1H), 7.81-7.77 (s, 1H), 7.72-7.68 (m, 1H),7.45-7.42 (m, 3H), 7.21-7.18 (m, 2H), 5.48-5.47 (s, 2H), 4.47-4.45 (m,2H), 4.18-4.12 (m, 3H), 3.69-3.51 (m, 4H), 1.62-1.52 (m, 6H), 1.24-1.22(s, 3H), 1.00-0.98 (s, 3H); MS (ES+): 571 (M+1).

Preparation of(S)-5-amino-1-(2-((2-((1-(3-chloro-2-fluorophenyl)-2-hydroxyethyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(328g) Step-1: Preparation of(S)-2-((tert-butyldimethylsilyl)oxy)-1-(3-chloro-2-fluorophenyl)ethanamine(328b)

To a solution of (S)-2-amino-2-(3-chloro-2-fluorophenyl)ethanol (328a)(1.05 g, 5.54 mmol) in DCM (50 mL) and DMF (5 mL) was added TBS-C₁(1.002 g, 6.65 mmol), Imidazole (0.528 g, 7.75 mmol) and stirred at RTfor 3h. The solid obtained was collected by filtration washed with DCM(2×4 mL) and dried under vacuum to afford(S)-2-((tert-butyldimethylsilyl)oxy)-1-(3-chloro-2-fluorophenyl)ethanamine(328b) (1.3 g, 77% yield) as a white solid; MS (ES+): 304.4 (M+1).

Step-2: Preparation of(S)—N-(2-((tert-butyldimethylsilyl)oxy)-1-(3-chloro-2-fluorophenyl)ethyl)-2-chloroacetamide(328c)

To a biphasic solution of(S)-2-(tert-butyldimethylsilyloxy)-1-(3-chloro-2-fluorophenyl)ethanamine(328b) (1.3 g, 4.28 mmol) in EtOAc (80 mL) and sat. NaHCO₃ solution (80mL) was added Chloroacetyl chloride (0.514 mL, 6.42 mmol) and stirred atRT for 16h. Layers were separated, aqueous layer was extracted withEtOAc (40 mL) and combined organics were washed with brine, dried,filtered, concentrated and purified by flash chromatography [silica gel24 g, EtOAc in hexanes 0 to 60% as eluents] to afford(S)—N-(2-(tert-butyldimethylsilyloxy)-1-(3-chloro-2-fluorophenyl)ethyl)-2-chloroacetamide(328c) (1.3 g, 80% yield) as a colorless thick syrup; ¹H NMR (300 MHz,DMSO-d₆) δ 8.75 (d, J=8.1 Hz, 1H), 7.51 (ddd, J=7.9, 7.1, 1.7 Hz, 1H),7.38 (ddd, J=8.1, 6.5, 1.7 Hz, 1H), 7.23 (td, J=7.9, 1.0 Hz, 1H), 5.18(q, J=6.7 Hz, 1H), 4.13 (s, 2H), 3.85-3.68 (m, 2H), 0.77 (s, 9H), −0.06(s, 3H), −0.10 (s, 3H); MS (ES+): 380.4 (M+1), 402.4 (M+Na), MS (ES−):414.3, 416.5 (M+Cl).

Step-3: Preparation of(S)—N-(2-((tert-butyldimethylsilyl)oxy)-1-(3-chloro-2-fluorophenyl)ethyl)-2-(cyclopropylamino)acetamide(328d)

To a solution of(S)—N-(2-(tert-butyldimethylsilyloxy)-1-(3-chloro-2-fluorophenyl)ethyl)-2-chloroacetamide(328c) in THF (30 mL) was added Cyclopropyl amine (0.723 mL, 10.25 mmol)and stirred at RT for 2 days. Mixture was poured into sat. NaHCO₃solution (60 mL) and resultant suspension extracted with EtOAc (2×50mL). The combined organics were washed with brine, dried (MgSO₄),filtered, concentrated and purified by column chromatography [silica gel24 g, EtOAc in hexane as eluents 0 to 100%] to afford(S)—N-(2-(tert-butyldimethylsilyloxy)-1-(3-chloro-2-fluorophenyl)ethyl)-2-(cyclopropylamino)acetamide(328d) (0.7 g, 51% yield) as a thick syrup; ¹H NMR (300 MHz, DMSO-d₆) δ8.28 (d, J=8.3 Hz, 1H), 7.53-7.44 (m, 1H), 7.39-7.30 (m, 1H), 7.25-7.17(m, 1H), 5.25-5.14 (m, 1H), 3.76 (d, J=5.8 Hz, 2H), 3.17 (d, J=1.2 Hz,2H), 2.14-2.06 (m, 1H), 0.77 (s, 9H), 0.39-0.30 (m, 2H), 0.29-0.22 (m,2H), −0.09 (s, 3H), −0.10 (s, 3H); MS (ES+): 401.5 (M+1), MS (ES−):435.4 (M+Cl).

Step-4: Preparation of(S)-1-(6-(3-chloro-2-fluorophenyl)-10-cyclopropyl-2,2,3,3-tetramethyl-8,11-dioxo-4-oxa-7,10-diaza-3-siladodecan-12-yl)-5-nitro-1H-indazole-3-carboxamide(328e)

Reaction of(S)—N-(2-(tert-butyldimethylsilyloxy)-1-(3-chloro-2-fluorophenyl)ethyl)-2-(cyclopropylamino)acetamide(328d) (200 mg, 0.50 mmol) with2-(3-carbamoyl-5-nitro-1H-indazol-1-yl)acetic acid (267c) (145 mg, 0.55mmol) according to the procedure reported in step-3 of Scheme 2 gaveafter workup and purification by flash column chromatography [silica gel12 g, DMA80 in DCM 0 to 30% as eluents](S)-1-(6-(3-chloro-2-fluorophenyl)-10-cyclopropyl-2,2,3,3-tetramethyl-8,11-dioxo-4-oxa-7,10-diaza-3-siladodecan-12-yl)-5-nitro-1H-indazole-3-carboxamide(328e) (0.216 g, 67% yield) as white solid; ¹H NMR (300 MHz, DMSO-d₆) δ9.05 (dd, J=2.3, 0.6 Hz, 1H), 8.54 (d, J=8.1 Hz, 1H), 8.26 (dd, J=9.3,2.3 Hz, 1H), 8.06 (s, 1H), 7.89 (dd, J=9.3, 0.7 Hz, 1H), 7.67 (s, 1H),7.51-7.41 (m, 1H), 7.36-7.27 (m, 1H), 7.16 (t, J=7.9 Hz, 1H), 5.84-5.66(m, 2H), 5.16 (q, J=7.0 Hz, 1H), 4.11-3.91 (m, 2H), 3.79-3.59 (m, 2H),3.09-2.95 (m, 1H), 1.03-0.92 (m, 2H), 0.92-0.83 (m, 2H), 0.74 (s, 9H),−0.08 (s, 3H), −0.13 (s, 3H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.35; MS(ES−): 681.5 (M−1).

Step-5: Preparation of(S)-1-(2-((2-((1-(3-chloro-2-fluorophenyl)-2-hydroxyethyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-nitro-1H-indazole-3-carboxamide(328f)

Compound 328f was prepared from(5)-1-(6-(3-chloro-2-fluorophenyl)-10-cyclopropyl-2,2,3,3-tetramethyl-8,11-dioxo-4-oxa-7,10-diaza-3-siladodecan-12-yl)-5-nitro-1H-indazole-3-carboxamide(328e) (0.21 g, 0.324 mmol) and TBAF (0.127 g, 0.487 mmol) according tothe procedure reported in step-2 of Scheme 301. This gave after workupand purification by flash chromatography [silica gel 4 g, DMA80 in DCM,0 to 20% as eluents](S)-1-(2-((2-((1-(3-chloro-2-fluorophenyl)-2-hydroxyethyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-nitro-1H-indazole-3-carboxamide(328f) (0.15 g, 87% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ9.05 (dd, J=2.3, 0.6 Hz, 1H), 8.54 (d, J=7.9 Hz, 1H), 8.26 (dd, J=9.3,2.3 Hz, 1H), 8.07 (s, 1H), 7.89 (dd, J=9.3, 0.7 Hz, 1H), 7.66 (s, 1H),7.49-7.40 (m, 1H), 7.32-7.23 (m, 1H), 7.17-7.10 (m, 1H), 5.84-5.65 (m,2H), 5.12-5.02 (m, 2H), 4.02 (s, 2H), 3.54 (t, J=6.0 Hz, 2H), 3.07-2.94(m, 1H), 1.03-0.92 (m, 2H), 0.92-0.82 (m, 2H); 19F NMR (282 MHz,DMSO-d₆) δ −121.91; MS (ES−): 531.4 (M−1), 567.5 (M+Cl).

Step-6: Preparation of(S)-5-amino-1-(2-((2-((1-(3-chloro-2-fluorophenyl)-2-hydroxyethyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(328g)

To a solution of(S)-1-(2-((2-((1-(3-chloro-2-fluorophenyl)-2-hydroxyethyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-nitro-1H-indazole-3-carboxamide(328f) (0.12 g, 0.225 mmol) in EtOH (3 mL) was added a solution ofAmmonium chloride (0.241 g, 4.50 mmol) in Water (3 mL) followed by Iron(0.126 g, 2.252 mmol) and mixture was stirred at 60° C. for 4h. Mixturewas filtered over Celite pad, washed with EtOH (3×5 mL) and water (3×5mL). The combined filtrate was concentrated partially and resultantresidue was partitioned between brine (60 mL) and EtOAc (80 mL), layerswere separated, aqueous layer was extracted with EtOAc (40 mL). Thecombined organics were washed with brine, dried, filtered, concentratedand purified by column chromatography [silica gel 4 g, DMA80 in DCM 0 to30% as eluents] to afford(S)-5-amino-1-(2-((2-((1-(3-chloro-2-fluorophenyl)-2-hydroxyethyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(328g) (0.015 g, 13% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆)δ 8.52 (d, J=7.8 Hz, 1H), 7.54-7.40 (m, 2H), 7.34-7.22 (m, 3H),7.21-7.08 (m, 2H), 6.78 (dd, J=8.8, 2.1 Hz, 1H), 5.57-5.39 (m, 2H),5.14-4.99 (m, 4H), 4.00 (s, 2H), 3.54 (t, J=6.0 Hz, 2H), 3.04-2.90 (m,1H), 1.01-0.77 (m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.91; MS (ES+):503.4 (M+1), 525.4 (M+Na), MS (ES−): 501.4 (M−1), 537.5 (M+Cl).

Preparation of(R)-1-(2-((2-((3-(3-chloropyridin-4-yl)-2-fluorophenyl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(329f) Step-1: Preparation of (R)-ethyl2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)-amino)acetate (329a)

To a solution of (R)-1-((tert-butyldimethylsilyl)oxy)propan-2-amine(314f) (8 g, 42.2 mmol) in THF (50 mL) added ethyl 2-bromoacetate (45a)(7.06 g, 42.2 mmol), TEA (7.07 mL, 50.7 mmol) and mixture was stirred atRT for 20h. Mixture was poured into sat. NaHCO₃ solution (100 mL) andresultant mixture was extracted with EtOAc (2×80 mL). The combinedorganics were washed with brine, dried, filtered, concentrated to afford(R)-ethyl 2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)amino)acetate(329a) (11 g, 95% yield) as a colorless liquid; ¹H NMR (300 MHz, CDCl₃)δ 4.18 (qd, J=7.2, 1.1 Hz, 2H), 3.58-3.33 (m, 4H), 2.83-2.68 (m, 1H),2.16 (s, 1H), 1.27 (t, J=7.1 Hz, 3H), 0.98 (d, J=6.4 Hz, 3H), 0.90 (s,9H), 0.05 (d, J=1.4 Hz, 6H).

Step-2: Preparation of (R)-ethyl2-(N-(1-((tert-butyldimethylsilyl)oxy)propan-2-yl)-2-(3-carbamoyl-1H-indazol-1-yl)acetamido)acetate(329b)

Reaction of (R)-ethyl2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)-amino)acetate (329a)(2.0 g, 7.26 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)acetic acid (2e)(1.91 g, 8.71 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup and purification by flash columnchromatography [silica gel 40 g, EtOAc in hexanes 0 to 100% as eluents](R)-ethyl2-(N-(1-((tert-butyldimethylsilyl)oxy)propan-2-yl)-2-(3-carbamoyl-1H-indazol-1-yl)acetamido)acetate(329b) (1.5 g, 3.15 mmol, 43.3% yield) as colorless foam; MS (ES+):477.5 (M+1), 499.5 (M+Na), MS (ES−): 511.5 (M+Cl).

Step-3: Preparation of(R)-2-(N-(1-((tert-butyldimethylsilyl)oxy)propan-2-yl)-2-(3-carbamoyl-1H-indazol-1-yl)acetamido)aceticacid (329c)

Hydrolysis of ester of (R)-ethyl2-(N-(1-((tert-butyldimethylsilyl)oxy)propan-2-yl)-2-(3-carbamoyl-1H-indazol-1-yl)acetamido)acetate(329b) (1.5 g, 3.15 mmol) according to the procedure reported in step-2of Scheme 129 gave after workup(R)-2-(N-(1-((tert-butyldimethylsilyl)oxy)propan-2-yl)-2-(3-carbamoyl-1H-indazol-1-yl)acetamido)aceticacid (329c) (1.1 g, 78% yield) as a white solid; MS (ES+): 471.5 (M+Na),MS (ES−): 447.4 (M−1)

Step-4: Preparation of 3-(3-chloropyridin-4-yl)-2-fluoroaniline (329d)

To a degassed solution of 3-bromo-2-fluoroaniline (282a) (2.415 g, 12.71mmol), 3-chloropyridin-4-ylboronic acid (2.00 g, 12.71 mmol) in ethyleneglycol dimethyl ether (50 mL) was added a solution of potassiumbicarbonate (4.45 g, 44.5 mmol) in water (2.00 mL) followed by(Pd(dppf)Cl₂ (0.930 g, 1.271 mmol) and mixture was stirred at 80° C. for17 h. The reaction mixture was cooled to room temperature, diluted withwater (100 mL) and extracted with ethyl acetate (2×100 mL). The combinedorganics were dried, filtered, concentrated and purified bychromatography [silica gel 24 g, eluting with EtOAc in hexanes from 0 to50%] to afford 3-(3-chloropyridin-4-yl)-2-fluoroaniline (329d) (0.189 g,7% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 8.75 (d, J=0.6Hz, 1H), 8.59 (d, J=4.9 Hz, 1H), 7.46 (dd, J=5.0, 0.6 Hz, 1H), 6.99 (td,J=7.7, 0.7 Hz, 1H), 6.93-6.80 (m, 1H), 6.54-6.41 (m, 1H), 5.36 (s, 2H,D₂O exchangeable); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −137.11; MS (ES+): 223.2(M+1).

Step-5: Preparation of(R)-1-(2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)(2-((3-(3-chloropyridin-4-yl)-2-fluorophenyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(329e)

Reaction of(R)-2-(N-(1-((tert-butyldimethylsilyl)oxy)propan-2-yl)-2-(3-carbamoyl-1H-indazol-1-yl)acetamido)aceticacid (329c) (0.13 g, 0.29 mmol) with3-(3-chloropyridin-4-yl)-2-fluoroaniline (329d) (0.065 g, 0.29 mmol)(45e) (54 mg, 0.379 mmol), according to the procedure reported in step-3of Scheme 2 gave after workup and purification by flash columnchromatography [Silica gel, 4 g eluting with EtOAc in hexanes 0 to 100%as eluents] of (R)-1-(2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)(2-((3-(3-chloropyridin-4-yl)-2-fluorophenyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(329e) (0.06 g, 32% yield) as colorless foam; MS (ES+): 653.6 (M+1),675.5 (M+Na).

Step-6: Preparation of(R)-1-(2-((2-((3-(3-chloropyridin-4-yl)-2-fluorophenyl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(329f)

Compound 329f was prepared from(R)-1-(2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)(2-((3-(3-chloropyridin-4-yl)-2-fluorophenyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(329e) (0.06 g, 0.092 mmol) and TBAF (0.072 g, 0.276 mmol) according tothe procedure reported in step-2 of Scheme 301. This gave after workupand purification by flash chromatography [silica gel 4 g, DMA80 in DCM,0 to 40% aseluents](R)-1-(2-((2-((3-(3-chloropyridin-4-yl)-2-fluorophenyl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(329f) (0.035 g, 71% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆)(a mixture of two rotamers) δ 10.35 and 10.02 (2s, 1H), 8.81 and 8.79(2s, 1H), 8.69-8.59 (m, 1H), 8.21-8.12 (m, 1H), 8.02 (t, J=7.7 Hz, 1H),7.72 and 7.68 (2s, 1H), 7.62-7.09 (m, 7H), 5.75-5.57 and 5.53-5.46 (2m,2H), 5.43 and 4.83 (2t, J=5.4 Hz, 1H) 4.61-4.40 and 4.30-4.18 (2m, 1H),4.19 and 3.97 (2d, J=16.6 Hz, 2H), 3.58-3.42 (m, 2H), 1.19 and 1.04 (2d,J=6.9 Hz, 3H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −126.30, −126.74; MS (ES+):539.4 (M+1), 561.5 (M+Na), MS (ES−): 537.5 (M−1), 573.5 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-6-hydroxy-1H-indazole-3-carboxamide(330b) Step 1: Preparation of2-(3-carbamoyl-6-hydroxy-1H-indazol-1-yl)acetic acid (330a)

Reaction of tert-butyl 2-(3-carbamoyl-6-hydroxy-1H-indazol-1-yl)acetate(301e) (50 mg, 0.172 mmol, crude) with 2,2,2-trifluoroacetic acid (0.2mL, 2.57 mmol) according to the procedure reported in step-2 of Scheme 2gave after workup 2-(3-carbamoyl-6-hydroxy-1H-indazol-1-yl)acetic acid(330a) which was used as such for next step.

Step 2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-6-hydroxy-1H-indazole-3-carboxamide(330b)

Reaction of 2-(3-carbamoyl-6-hydroxy-1H-indazol-1-yl)acetic acid (330a)(0.172 mmol, crude) withN-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide (0.066 g, 0.26mmol) (10b) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column chromatography[silica gel, eluting with dichloromethane/methanol (1:0 to 92:8)]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-6-hydroxy-1H-indazole-3-carboxamide(330b) (26 mg, 32% for two steps) as an off-white solid; ¹H NMR (300MHz, DMSO-d₆) δ 9.80 (s, 1H), 8.50 (t, J=5.8 Hz, 1H), 7.96-7.87 (m, 1H),7.59 (s, 1H), 7.50-7.38 (m, 1H), 7.32-7.19 (m, 2H), 7.13 (t, J=7.9 Hz,1H), 6.84-6.75 (m, 2H), 5.50 (s, 2H), 4.33 (d, J=5.7 Hz, 2H), 3.98 (s,2H), 3.11-2.96 (m, 1H), 1.00-0.85 (m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.62; MS (ES−): 472.4 & 474.5 (M−1).

Preparation of(R)-1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-5-nitro-1H-indazole-3-carboxamide(331b) Step-1: Preparation of(R)-1-(2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)(2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)amino)-2-oxoethyl)-5-nitro-1H-indazole-3-carboxamide(331a)

Compound 331b was prepared from(R)-2-(1-(tert-butyldimethylsilyloxy)propan-2-ylamino)-N-(2′-chloro-2-fluorobiphenyl-3-yl)acetamide(314g) (1.00 g, 2.22 mmol) by reaction with2-(3-carbamoyl-5-nitro-1H-indazol-1-yl)acetic acid (267d) (703 mg, 2.66mmol) according to the procedure reported in step-3 of Scheme 2. Thisgave after workup and purification by flash column chromatography[Silica gel, 24 g eluting with ethyl acetate/methanol (9:1) in hexanesfrom 0-100%](R)-1-(2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)(2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)amino)-2-oxoethyl)-5-nitro-1H-indazole-3-carboxamide(331a) (494 mg, 32% yield) as a yellow solid; MS (ES+): 697.7 (M+1),719.5 (M+Na); MS (ES−): 695.5 (M−1).

Step-2: Preparation of(R)-1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-5-nitro-1H-indazole-3-carboxamide(331b)

Compound 331b was prepared from(R)-1-(2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)(2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)amino)-2-oxoethyl)-5-nitro-1H-indazole-3-carboxamide(331a) (106 mg, 0.15 mmol) and TBAF (60 mg, 0.228 mmol) according to theprocedure reported in step-2 of Scheme 301. This gave after workup andpurification by flash chromatography [First column; silica gel 12 g,eluting with methanol in DCM from 0-100%; second column, silica gel 12g, eluting with ethyl acetate/methanol (9:1) in hexanes from 0-100%](R)-1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-5-nitro-1H-indazole-3-carboxamide(331b) (61 mg, 69% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆,mixture of two rotamers) δ 10.30 & 9.95 (2s, 1H, D₂O exchangeable),9.08-9.03 (m, 1H), 8.33 (dd, J=9.3, 2.3 Hz) & 8.22 (dd, J=9.3, 2.3 Hz)(2dd, 1H), 8.15-7.91 (m, 2H, D₂O exchangeable 1H), 7.82 (d, J=9.3 Hz) &7.73 (d, J=9.3 Hz) (2d, 1H), 7.68 (bs, 1H, D₂O exchangeable), 7.64-7.56(m, 1H), 7.54-7.37 (m, 3H), 7.32 (t, J=7.9 Hz) & 7.23 (t, J=7.9 Hz) (2t,1H), 7.19-7.03 (m, 1H), 5.92-5.69 (m, 1H), 5.61 (s, 1H), 5.42 (t, J=5.6Hz) & 4.83 (t, J=5.5 Hz) (2t, 1H, D₂O exchangeable), 4.61-3.90 (m, 3H),3.65-3.45 (m, 2H), 1.21 (d, J=6.5 Hz) & 1.04 (d, J=6.9 Hz) (2d, 3H); ¹⁹FNMR (282 MHz, DMSO-d₆) δ −126.53, −126.90; MS (ES+): 583.4 (M+1), 606.4,607.4 (M+Na); MS (ES−): 581.5, 583.5 (M−1).

Preparation of(R)-1-(2-((2-((3-chloro-2-fluoro-5-morpholinobenzyl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(332c) Step-1: Preparation of(R)-1-(2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)(2-((3-chloro-2-fluoro-5-morpholinobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(332b)

Reaction of(R)-2-(N-(1-((tert-butyldimethylsilyl)oxy)propan-2-yl)-2-(3-carbamoyl-1H-indazol-1-yl)acetamido)aceticacid (329c) (100 mg, 0.223 mmol) with(3-chloro-2-fluoro-5-morpholinophenyl)methanamine hydrochloride (332a)(0.063 g, 0.223 mmol, prepared according to the procedure reported byAltmann, Eva et al; in PCT Int. Appl. (2012), WO 2012093101) accordingto the procedure reported in step-3 of Scheme 2 gave after workup andpurification by flash column chromatography [Silica gel, 4 g elutingwith DMA80 in DCM 0 to 30% as eluents](R)-1-(2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)(2-((3-chloro-2-fluoro-5-morpholinobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(332b) (100 mg, 66% yield) as colorless foam; MS (ES−): 673.6 (M−1).

Step-2: Preparation of(R)-1-(2-((2-((3-chloro-2-fluoro-5-morpholinobenzyl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)-amino)-2-oxo ethyl)-1H-indazole-3-carboxamide (332c)

Compound 332c was prepared from of(R)-1-(2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)(2-((3-chloro-2-fluoro-5-morpholinobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(332b) (100 mg, 0.148 mmol) and TBAF (0.077 g, 0.296 mmol) according tothe procedure reported in step-2 of Scheme 301. This gave after workupand purification by flash chromatography [silica gel 4 g, DMA80 in DCM,0 to 40% as eluents](R)-1-(2-((2-((3-chloro-2-fluoro-5-morpholinobenzyl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide (332c) (66 mg,79% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) (a mixture of tworotamers) δ 8.82 and 8.58 (2t, J=5.9 Hz, 1H), 8.21-8.14 (m, 1H),7.76-7.17 (m, 5H), 7.03-6.63 (m, 2H), 5.70-5.55 and 5.44-5.34 (2m, 2H),5.50 and 4.81 (2t, J=6.0 Hz, 1H), 4.49-3.12 (m, 11H), 3.05-2.94 and2.81-2.71 (2m, 4H), 1.17 (d, J=6.5 Hz) and 1.00-0.94 (m) (3H); ¹⁹F NMR(282 MHz, DMSO-d₆) (a mixture of two rotamers) δ −134.26, −135.26; MS(ES−): 595.5 (M+Cl).

Preparation of2-(3-acetyl-5-(6-morpholinopyridin-3-yl)-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(333a)

Reaction of2-(3-acetyl-5-bromo-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(158a) (0.12 g, 0.224 mmol) with 6-morpholinopyridin-3-ylboronic acid(0.056 g, 0.269 mmol) according to the procedure reported in Scheme 78gave after workup and purification by reverse phase columnchromatography [silica gel 50 g, Acetonitrile in water (0.1% TFA) 0 to50% as eluents]2-(3-acetyl-5-(6-morpholinopyridin-3-yl)-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(333a) (0.055 g, 40% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆)δ 8.53-8.45 (m, 2H), 8.31-8.29 (m, 1H), 7.93 (dd, J=8.8, 2.6 Hz, 1H),7.81-7.70 (m, 2H), 7.49-7.41 (m, 1H), 7.27-7.18 (m, 1H), 7.14-7.05 (m,1H), 6.97 (d, J=8.9 Hz, 1H), 5.78 (s, 2H), 4.34 (d, J=5.7 Hz, 2H), 4.00(s, 2H), 3.78-3.68 (m, 4H), 3.55-3.46 (m, 4H), 3.20-3.07 (m, 1H), 2.63(s, 3H), 1.10-0.98 (m, 2H), 0.98-0.85 (m, 2H); ¹⁹F NMR (282 MHz,DMSO-d₆) δ −121.58; MS (ES+): 619.0 (M+1), 641.5 (M+Na).

Preparation of2-(3-acetyl-5-(6-(4-methylpiperazin-1-yl)pyridin-3-yl)-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(334a)

Reaction of2-(3-acetyl-5-bromo-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(158a) (0.12 g, 0.224 mmol)6-(4-methylpiperazin-1-yl)pyridin-3-ylboronic acid hydrochloride (0.058g, 0.224 mmol) according to the procedure reported in Scheme 78 gaveafter workup and purification by reverse phase column chromatography[silica gel 50 g, Acetonitrile in water (0.1% TFA) 0 to 50% as eluents]2-(3-acetyl-5-(6-(4-methylpiperazin-1-yl)pyridin-3-yl)-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)-N-cyclopropylacetamide(334a) (0.033 g, 23% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆)δ 8.54-8.45 (m, 2H), 8.33-8.27 (m, 1H), 7.90 (dd, J=8.9, 2.5 Hz, 1H),7.80-7.69 (m, 2H), 7.50-7.41 (m, 1H), 7.27-7.19 (m, 1H), 7.15-7.06 (m,1H), 6.98 (d, J=8.8 Hz, 1H), 5.78 (s, 2H), 4.34 (d, J=5.7 Hz, 2H), 4.00(s, 2H), 3.58 (td, J=12.7, 11.0, 4.4 Hz, 4H), 3.21-3.07 (m, 1H), 2.63(s, 3H), 2.53 (brs, 4H), 2.30 (s, 3H), 1.10-0.98 (m, 2H), 0.98-0.85 (m,2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.58; MS (ES+): 632.6 (M+1), 654.6(M+Na); MS (ES−): 666.6 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-hydroxy-1H-indazole-3-carboxamide(335b) Step-1: Preparation of2-(3-carbamoyl-5-hydroxy-1H-indazol-1-yl)acetic acid (335a)

Reaction of tert-butyl 2-(3-carbamoyl-5-hydroxy-1H-indazol-1-yl)acetate(214b) (260 mg, 0.89 mmol) with 2,2,2-trifluoroacetic acid (1.03 mL,13.39 mmol) according to the procedure reported in step-2 of Scheme 2gave after workup 2-(3-carbamoyl-5-hydroxy-1H-indazol-1-yl)acetic acid(335a), which was used as such for next step.

Step 2 Preparation of1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-hydroxy-1H-indazole-3-carboxamide(335b)

Reaction of 2-(3-carbamoyl-5-hydroxy-1H-indazol-1-yl)acetic acid (335a)(210 mg, 0.89 mmol, crude) withN-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide (10b) (344 mg,1.34 mmol according to the procedure reported in step-3 of Scheme 2 gaveafter workup and purification by flash column chromatography [silicagel, eluting with dichloromethane/methanol (1:0 to 19:1)]1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-hydroxy-1H-indazole-3-carboxamide(335b) (101 mg, 24%) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 9.36(s, 1H), 8.49 (t, J=5.9 Hz, 1H), 7.57 (s, 1H), 7.51-7.42 (m, 3H),7.28-7.18 (m, 2H), 7.12 (td, J=7.9, 1.0 Hz, 1H), 6.92 (dd, J=9.0, 2.4Hz, 1H), 5.57 (s, 2H), 4.33 (d, J=5.7 Hz, 2H), 3.98 (s, 2H), 3.13-2.92(m, 1H), 1.03-0.80 (m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.58; MS(ES+): 496.3 & 498.3 (M+Na); MS (ES−): 472.4 & 474.4 (M−1).

Preparation of5-chloro-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(336b) Step 1: Preparation of tert-butyl2-(5-chloro-3-cyano-1H-indazol-1-yl)acetate (336b)

Reaction of 5-chloro-1H-indazole-3-carbonitrile (336a) (500 mg, 2.67mmol) with tert-butyl 2-bromoacetate (0.474 mL, 3.21 mmol) according tothe procedure reported in step-1 of Scheme 43 gave after workuptert-butyl 2-(5-chloro-3-cyano-1H-indazol-1-yl)acetate (336b) (1.013 g)as a brown semi-solid, which was used as such for next step. MS (ES−):290.4 & 292.3 (M−1).

Step 2: Preparation of 2-(5-chloro-3-cyano-1H-indazol-1-yl)acetic acid(336c)

Reaction of tert-butyl 2-(5-chloro-3-cyano-1H-indazol-1-yl)acetate(336b) (0.779 g, 2.67 mmol, crude) with 2,2,2-trifluoroacetic acid (2.06mL, 26.7 mmol) according to the procedure reported in step-2 of Scheme 2gave after workup 2-(5-chloro-3-cyano-1H-indazol-1-yl)acetic acid(336c), which was used as such for next step.

Step 3: Preparation ofN-(2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)-2-(5-chloro-3-cyano-1H-indazol-1-yl)-N-cyclopropylacetamide(336d)

Reaction of 2-(5-chloro-3-cyano-1H-indazol-1-yl)acetic acid (336c)(0.629 g, 2.67 mmol, crude) withN-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide (10b) (0.82 g,3.20 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column chromatography[silica gel with hexanes/10% methanol in ethyl acetate (1:0 to 1:1)]N-(2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)-2-(5-chloro-3-cyano-1H-indazol-1-yl)-N-cyclopropylacetamide(336d) (479 mg, 38% for three steps) as a yellow solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.47 (t, J=5.9 Hz, 1H), 8.06 (dd, J=1.9, 0.7 Hz, 1H), 7.89(dd, J=9.1, 0.8 Hz, 1H), 7.60 (dd, J=9.0, 1.9 Hz, 1H), 7.50-7.42 (m,1H), 7.25-7.18 (m, 1H), 7.13-7.07 (m, 1H), 5.81 (s, 2H), 4.33 (d, J=5.7Hz, 2H), 3.97 (s, 2H), 3.16-2.98 (m, 1H), 1.08-0.82 (m, 4H); ¹⁹F NMR(282 MHz, DMSO-d₆) δ −121.57; MS (ES+): 474.4 (M+1).

Step 4: Preparation of5-chloro-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)-(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(336e)

Reaction ofN-(2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)-2-(5-chloro-3-cyano-1H-indazol-1-yl)-N-cyclopropylacetamide(336d) (369 mg, 0.778 mmol) with hydrogen peroxide (0.275 mL, 3.11 mmol)according to the procedure reported in Scheme 65 gave after workup andpurification by flash column chromatography [silica gel with hexanes/10%methanol in ethyl acetate (1:0 to 1:1)]5-chloro-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)-(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(336e) (197 mg, 51%) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 8.50(t, J=5.8 Hz, 1H), 8.16 (dd, J=2.1, 0.7 Hz, 1H), 7.82 (s, 1H), 7.73 (dd,J=9.0, 0.7 Hz, 1H), 7.50-7.42 (m, 3H), 7.26-7.17 (m, 1H), 7.11 (td,J=7.8, 1.0 Hz, 1H), 5.68 (s, 2H), 4.33 (d, J=5.7 Hz, 2H), 3.98 (s, 2H),3.14-2.93 (m, 1H), 1.05-0.81 (m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.56; MS (ES+): 514.3 & 516.3 (M+Na); MS (ES−): 490.3 (M−1).

Preparation of(R)-1-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(337d) Step-1: Preparation of N-(6-bromopyridin-2-yl)-2-chloroacetamide(337a)

Compound 337a was prepared from 6-bromopyridin-2-amine (2a) (2 g, 11.56mmol) and Chloroacetyl chloride (1.852 mL, 23.12 mmol), according to theprocedure reported in step-1 of Scheme 35. This gave after workup andpurification by flash column chromatography [silica gel 40 g,EtOAc-hexane 0 to 40% as eluents] to affordN-(6-bromopyridin-2-yl)-2-chloroacetamide (337a) (2.3 g, 80% yield) as awhite solid; ¹H NMR (300 MHz, DMSO-d₆) δ 11.19 (s, 1H), 8.06 (dd, J=8.2,0.7 Hz, 1H), 7.86-7.67 (m, 1H), 7.39 (dd, J=7.7, 0.7 Hz, 1H), 4.34 (s,2H).

Step-2: Preparation of(R)—N-(6-bromopyridin-2-yl)-2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)-amino)acetamide(337b)

Compound 337b was prepared fromN-(6-bromopyridin-2-yl)-2-chloroacetamide (337a) (0.5 g, 2.0 mmol) and(R)-1-((tert-butyldimethylsilyl)oxy)propan-2-amine (314f) (0.38 g, 2.0mmol) according to the procedure reported in step-1 of Scheme 35. Thisgave after workup and purification by flash column chromatography[silica gel 24 g, EtOAc-DCM 10 to 100% as eluents](R)—N-(6-bromopyridin-2-yl)-2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)-amino)acetamide(337b) (0.5 g, 62% yield) as thick syrup; ¹H NMR (300 MHz, DMSO-d₆) δ10.51 (s, 1H), 8.10 (dd, J=8.2, 0.7 Hz, 1H), 7.74 (t, J=7.9 Hz, 1H),7.34 (dd, J=7.7, 0.7 Hz, 1H), 3.44 (d, J=5.8 Hz, 2H), 3.41-3.37 (m, 1H),3.35 (s, 2H), 2.66 (q, J=6.1 Hz, 1H), 0.94 (d, J=6.4 Hz, 3H), 0.85 (s,9H), 0.03 (s, 3H), −0.00 (s, 3H); MS (ES+): 402.4, 403.3 (M+1), MS(ES−): 436.3, 438.4 (M+Cl).

Step-3: Preparation of(R)-1-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(1-((tert-butyldimethylsilyl)oxy)propan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(337c)

Reaction of(R)—N-(6-bromopyridin-2-yl)-2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)-amino)acetamide(337b) (200 mg, 0.50 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (163 mg, 0.75 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica gel 12 g, DMA80 in DCM 0 to 20% as eluents](R)-1-(2-((2-((6-bromopyridin-2-yl)amino)-2-carboxamide (337c) (0.19 g,63% yield) as a colorless foam; MS (ES+): 603.5, 605.5 (M+1), MS (ES+):601.5, 603.5 (M−1).

Step-4: Preparation of(R)-1-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(337d)

Compound 337d was prepared from(R)-1-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(1-((tert-butyldimethylsilyl)oxy)propan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(337c) (0.07 g, 0.12 mmol) and TBAF (0.061 g, 0.232 mmol) according tothe procedure reported in step-2 of Scheme 301. This gave after workupand purification by flash chromatography [silica gel 4 g, DMA80 in DCM,0 to 30% as eluents](R)-1-(2-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(337d) (0.038 g, 67% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆)(a mixture of two rotamers) δ 11.19 and 10.90 (2s, 1H), 8.21-8.12 (m,1H), 8.02 and 7.99 (2s, 1H), 7.86-7.17 (m, 7H), 5.75-5.57 (m) and 5.45(s, 2H), 5.35 and 4.77 (2t, J=5.5 Hz, 1H), 4.56-4.36 and 4.21 (2 m, 1H),4.15 and 3.93 (2d, J=16.7 Hz, 2H), 3.59-3.39 (m, 2H), 1.17 and 1.00 (2d,J=6.9 Hz, 3H); MS (ES+): 489.3, 491.3 (M+1), 511.3, 513.3 (M+Na), MS(ES−): 487.3, 489.3 (M−1).

Preparation of(R)-1-(2-((2-((2-fluoro-3-(3-methylpyridin-2-yl)phenyl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(338c) Step-1: Preparation of(R)-1-(2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)(2-((2-fluoro-3-(3-methylpyridin-2-yl)phenyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(338b)

Reaction of(R)-2-(N-(1-((tert-butyldimethylsilyl)oxy)propan-2-yl)-2-(3-carbamoyl-1H-indazol-1-yl)acetamido)aceticacid (329c) (0.1 g, 0.22 mmol) with2-fluoro-3-(3-methylpyridin-2-yl)aniline (338a) (0.045 g, 0.22 mmol;prepared according to the procedure reported by Altmann, Eva et al; inPCT Int. Appl., 2012093101, 12 Jul. 2012) according to the procedurereported in step-3 of Scheme 2 gave after workup and purification byflash column chromatography [Silica gel, 12 g eluting with DMA80 in DCM0 to 20% as eluents] to afford(R)-1-(2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)(2-((2-fluoro-3-(3-methylpyridin-2-yl)phenyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(338b) (0.045 g, 32% yield) as a colorless foam; MS (ES+): 633.5 (M+1),655.5 (M+Na).

Step-2: Preparation of(R)-1-(2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)(2-((2-fluoro-3-(3-methylpyridin-2-yl)phenyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(338c)

Compound 338c was prepared from(R)-1-(2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)(2-((2-fluoro-3-(3-methylpyridin-2-yl)phenyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(338b) (0.045 g, 0.071 mmol) and TBAF (0.037 g, 0.142 mmol) according tothe procedure reported in step-2 of Scheme 301. This gave after workupand purification by flash chromatography [silica gel 4 g, DMA80 in DCM,0 to 30% as eluents](R)-1-(2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)(2-((2-fluoro-3-(3-methylpyridin-2-yl)phenyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(338c) (0.028 g, 76% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆)(a mixture of two rotamers) δ 10.28 and 9.95 (2s, 1H), 8.53-8.47 (m,1H), 8.21-8.14 (m, 1H), 8.06-7.97 (m, 1H), 7.81-7.06 (m, 9H), 5.74-5.59(m) and 5.49 (s) (2H), 5.45 and 4.84 (t, J=5.5 Hz, 1H), 4.59-3.86 (m,3H), 3.62-3.38 (m, 2H), 2.20 and 2.14 (2s, 3H), 1.19 and 1.04 (2d, J=6.9Hz, 3H); ¹⁹F NMR (282 MHz, DMSO-d₆) (a mixture of two rotamers) δ−127.76, −128.34; MS (ES+) 519.4 (M+1), 541.4 (M+Na), MS (ES−) 517.5(M−1).

Preparation of(R)-1-(2-((2-((3-cyano-2-fluorobenzyl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(339d) Step-1: Preparation of 3-(aminomethyl)-2-fluorobenzonitrile(339b)

To a solution of 3-(bromomethyl)-2-fluorobenzonitrile (339a) (0.25 g,1.168 mmol) in DMSO (5 mL) was added Sodium azide (0.114 g, 1.752 mmol)and stirred at 50° C. for 16h. Mixture was partitioned between water (50mL) and EtOAc (60 mL) and Layers were separated. The aqueous layer wasextracted with EtOAc (40 mL) and the combined organics were washed withwater (50 mL), brine, dried, filtered and concentrated to afford azideas a pasty mass. This pasty mass was dissolved in Ethyl acetate (10 mL),added Palladium hydroxide on carbon (0.016 g, 0.117 mmol) and mixturewas stirred under Hydrogen atmosphere for 2 h. Mixture was filtered overa Celite pad, washed with EtOAc (2×5 mL) and filtrate was concentratedin vacuum to afford 3-(aminomethyl)-2-fluorobenzonitrile (339b) (0.13 g,74% yield) as off-white foam; ¹H NMR (300 MHz, DMSO-d₆) δ 7.92-7.83 (m,1H), 7.82-7.72 (m, 1H), 7.39 (t, J=7.7 Hz, 1H), 3.78 (s, 2H), 1.92 (d,J=30.5 Hz, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −115.06.

Step-2: Preparation of(R)-1-(2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)(2-((3-cyano-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(339c)

Reaction of(R)-2-(N-(1-((tert-butyldimethylsilyl)oxy)propan-2-yl)-2-(3-carbamoyl-1H-indazol-1-yl)acetamido)aceticacid (329c) (0.12 g, 0.268 mmol) with3-(aminomethyl)-2-fluorobenzonitrile (339b) (0.060 g, 0.401 mmol)according to the procedure reported in step-3 of Scheme 2 gave afterworkup and purification by flash column chromatography [Silica gel, 4 geluting with EtOAc in DCM 0 to 100% as eluents](R)-1-(2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)(2-((3-cyano-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(339c) (0.07 g, 45% yield) as a colorless foam; MS (ES+) 603.5 (M+Na).

Step-3: Preparation of(R)-1-(2-((2-((3-cyano-2-fluorobenzyl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxo ethyl)-1H-indazole-3-carboxamide (339d)

Compound 339d was prepared from(R)-1-(2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)(2-((3-cyano-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(339c) (0.07 g, 0.121) and TBAF (0.063 g, 0.241 mmol) according to theprocedure reported in step-2 of Scheme 301. This gave after workup andpurification by flash chromatography [silica gel 4 g, DMA80 in DCM, 0 to30% as eluents](R)-1-(2-((2-((3-cyano-2-fluorobenzyl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(339d) (0.025 g, 45% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆)(a mixture of two rotamers) δ 8.91 and 8.65 (2t, J=5.9 Hz, 1H),8.21-8.18 and 8.18-8.14 (2m, 1H), 7.89-7.73 (m, 1H), 7.69 (s, 1H),7.61-7.08 (m, 6H), 5.66-5.55 (m) and 5.41 (s) (2H), 5.48 and 4.80 (2t,J=5.7 Hz, 1H), 4.55-3.69 (m, 5H), 3.51-3.40 (m, 2H), 1.15 and 0.95 (2d,J=6.9 Hz, 3H); ¹⁹F NMR (282 MHz, DMSO-d₆) (a mixture of two rotamers) δ−113.49, −113.84; MS (ES+): 467.5 (M+1), 489.5 (M+Na), MS (ES−): 465.5(M−1), 501.5 (M+Cl).

Preparation of(R)-1-(2-((2-((2-fluoro-2′-methyl-[1,1′-biphenyl]-3-yl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(340c) Step-1: Preparation of 2-fluoro-2′-methyl-[1,1′-biphenyl]-3-amine(340a)

Compound 340a was prepared from 3-bromo-2-fluoroaniline (282a) (0.5 g,2.63 mmol) and o-tolylboronic acid (0.43 g, 3.16 mmol) according to theprocedure reported in step-4 of Scheme 329. This gave after workup andpurification by flash column chromatography [silica gel 12 g, EtOAc inhexanes 0 to 30% as eluents] 2-fluoro-2′-methyl-[1,1′-biphenyl]-3-amine(340a) (0.4 g, 76% yield) as a colorless liquid; ¹H NMR (300 MHz,DMSO-d₆) δ 7.33-7.18 (m, 3H), 7.18-7.11 (m, 1H), 6.95-6.86 (m, 1H), 6.77(td, J=8.3, 1.7 Hz, 1H), 6.36 (ddd, J=7.5, 6.5, 1.7 Hz, 1H), 5.18 (s,2H), 2.13 (s, 3H).

Step-2: Preparation of(R)-1-(2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)(2-((2-fluoro-2′-methyl-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(340b)

Reaction of(R)-2-(N-(1-((tert-butyldimethylsilyl)oxy)propan-2-yl)-2-(3-carbamoyl-1H-indazol-1-yl)acetamido)aceticacid (329c) (0.12 g, 0.27 mmol) with2-fluoro-2′-methyl-[1,1′-biphenyl]-3-amine (340a) (0.065 g, 0.32 mmol)according to the procedure reported in step-3 of Scheme 2 gave afterworkup and purification by flash column chromatography [Silica gel, 4 geluting with EtOAc in DCM 0 to 100% as eluents](R)-1-(2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)(2-((2-fluoro-2′-methyl-[1,1′-biphenyl]-3-yl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(340b) (0.09 g, 53% yield) as a colorless foam; MS (ES+): 654.6 (M+Na).

Step-3: Preparation of(R)-1-(2-((2-((2-fluoro-2′-methyl-[1,1′-biphenyl]-3-yl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(340c)

Compound 340c was prepared from(R)-1-(2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)(2-((2-fluoro-2′-methyl-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(340b) (0.09 g, 0.142 mmol) and TBAF (0.074 g, 0.285 mmol) according tothe procedure reported in step-2 of Scheme 301. This gave after workupand purification by flash chromatography [silica gel 4 g, DMA80 in DCM,0 to 30% as eluents](R)-1-(2-((2-((2-fluoro-2′-methyl-[1,1′-biphenyl]-3-yl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide (340c) (0.058g, 79% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) (a mixture oftwo rotamers) δ 10.25 and 9.92 (s, 1H), 8.21-8.13 (m, 1H), 8.05-7.97 and7.95-7.86 (2m, 1H), 7.73 and 7.68 (2s, 1H), 7.62-7.14 (m, 9H), 7.14-7.06and 7.05-6.97 (2m, 1H), 5.74-5.58 and 5.48 (m and s, 2H), 5.45 and 4.83(2t, J=5.5 Hz, 1H), 4.59-3.86 (m, 3H), 3.60-3.38 (m, 2H), 2.16 and 2.11(2s, 3H), 1.19 and 1.04 (2d, J=6.9 Hz, 3H); ¹⁹F NMR (282 MHz, DMSO-d₆)(a mixture of two rotamers) δ −127.21, −127.76; MS (ES+): 540.5 (M+Na):MS (ES−): 516.6 (M−1).

Preparation of(R)-5-amino-1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(341a)

Compound 341a was prepared from(R)-1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-5-nitro-1H-indazole-3-carboxamide(331b) (0.05 g, 0.086 mmol) according to the procedure reported instep-6 of Scheme 328. This gave after workup and purification by flashchromatography [silica gel 4 g, DMA80 in DCM 0 to 30% as eluents](R)-5-amino-1-(2-((2-((2′-chloro-2-fluoro-[1,1′-biphenyl]-3-yl)-amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(341a) (0.025 g, 53% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆)(a mixture of two rotamers) δ 10.26 and 9.97 (2s, 1H), 8.10-8.04 and8.01-7.93 (2m, 1H), 7.66-7.01 (m, 10H), 6.81 and 6.75 (2dd, J=8.9, 2.1Hz, 1H), 5.59-5.43 (m) and 5.33 (s) (2H), 5.39 and 4.82 (2t, J=5.5 Hz,1H), 5.03 and 5.02 (2s, 2H), 4.58-3.87 (m, 3H), 3.57-3.43 (m, 2H), 1.15and 1.03 (2d, J=6.9 Hz, 3H); ¹⁹F NMR (282 MHz, DMSO-d₆) (a mixture oftwo rotamers) δ −126.49, −127.01; MS (ES+): 575.4 (M+Na), MS (ES−):551.5 (M−1), 587.5 (M+Cl).

Preparation of5-acetyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)-amino)-2-oxo-ethyl)-1H-indazole-3-carboxamide(342d) Step 1: Preparation of ethyl2-(5-bromo-3-carbamoyl-1H-indazol-1-yl)acetate (342a)

Reaction of 5-bromo-1H-indazole-3-carboxamide (137b) (4.4 g, 18.33 mmol)with ethylbromoacetate (3.06 mL, 27.5 mmol) according to the procedurereported in step-1 of Scheme 43 gave after workup ethyl2-(5-bromo-3-carbamoyl-1H-indazol-1-yl)acetate (342a) (4.5 g, 75% yield)as a white solids; ¹H NMR (300 MHz, DMSO-d₆) δ 8.33 (dd, J=2.0, 0.7 Hz,1H), 7.84 (s, 1H), 7.78 (dd, J=9.0, 0.7 Hz, 1H), 7.62 (dd, J=9.0, 1.9Hz, 1H), 7.54 (s, 1H), 5.49 (s, 2H), 4.16 (q, J=7.1 Hz, 2H), 1.20 (t,J=7.2 Hz, 3H).

Step 2: Preparation of ethyl2-(5-acetyl-3-carbamoyl-1H-indazol-1-yl)acetate (342b)

Reaction of ethyl 2-(5-bromo-3-carbamoyl-1H-indazol-1-yl)acetate (342a)(200 mg, 0.613 mmol) with tributyl(1-ethoxyvinyl)stannane (0.267 mL,0.767 mmol) according to the procedure reported in step-1 and step-2 ofScheme 206 gave after workup and purification by flash columnchromatography [silica gel with hexanes/10% methanol in ethyl acetate(1:0 to 1:1)] ethyl 2-(5-acetyl-3-carbamoyl-1H-indazol-1-yl)acetate as awhite solid (342b) (58 mg, 33%). ¹H NMR (300 MHz, DMSO-d₆) δ 8.83 (dd,J=1.7, 0.8 Hz, 1H), 8.04 (dd, J=8.9, 1.6 Hz, 1H), 7.90 (s, 1H), 7.85(dd, J=9.0, 0.8 Hz, 1H), 7.61 (s, 1H), 5.53 (s, 2H), 4.17 (q, J=7.1 Hz,2H), 2.66 (s, 3H), 1.21 (t, J=7.1 Hz, 3H); MS (ES+): 312.4 (M+Na).

Step 3: Preparation of 2-(5-acetyl-3-carbamoyl-1H-indazol-1-yl)aceticacid (342c)

Reaction of ethyl 2-(5-acetyl-3-carbamoyl-1H-indazol-1-yl)acetate (342b)(54 mg, 0.187 mmol) with lithium hydroxide hydrate (47.0 mg, 1.120 mmol)according to the procedure reported in step-2 of Scheme 129 gave afterworkup and purification 2-(5-acetyl-3-carbamoyl-1H-indazol-1-yl)aceticacid (342c) (25 mg, 51%) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ13.40 (s, 1H), 8.88-8.78 (m, 1H), 8.03 (dd, J=8.9, 1.7 Hz, 1H), 7.90 (s,1H), 7.84 (d, J=9.0 Hz, 1H), 7.59 (s, 1H), 5.40 (s, 2H), 2.66 (s, 3H);MS (ES−): 260.3 (M−1).

Step 4: Preparation of5-acetyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)-(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(342d)

Reaction of 2-(5-acetyl-3-carbamoyl-1H-indazol-1-yl)acetic acid (342c)(23 mg, 0.088 mmol) withN-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide (10b) (33.9mg, 0.132 mmol) according to the procedure reported in step-3 of Scheme2 gave after workup and purification by flash column chromatography[silica gel with dichloromethane/methanol (1:0 to 19:1)]5-acetyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)-(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(342d) (19 mg, 43%). ¹H NMR (300 MHz, DMSO-d₆) δ 8.84-8.80 (m, 1H), 8.50(t, J=5.8 Hz, 1H), 7.98 (dd, J=8.9, 1.6 Hz, 1H), 7.89 (s, 1H), 7.80-7.70(m, 1H), 7.56 (s, 1H), 7.46 (td, J=7.6, 1.7 Hz, 1H), 7.28-7.18 (m, 1H),7.10 (td, J=7.9, 1.0 Hz, 1H), 5.72 (s, 2H), 4.33 (d, J=5.7 Hz, 2H), 3.99(s, 2H), 3.13-2.98 (m, 1H), 2.66 (s, 3H), 1.09-0.84 (m, 4H); ¹⁹F NMR(282 MHz, DMSO-d₆) δ −121.56; MS (ES+): 522.4 (M+Na); MS (ES−): 498.4(M−1).

Preparation of1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)-amino)-2-oxoethyl)-5-fluoro-1H-indazole-3-carboxamide(343b)

Reaction of 2-(3-carbamoyl-5-fluoro-1H-indazol-1-yl)acetic acid (343a)(30 mg, 0.126 mmol; prepared according to the procedure reported byAltmann, Eva et al; in PCT hit. Appl., 2014002054, 3 Jan. 2014) withN-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide (10b) (48.7mg, 0.190 mmol) according to the procedure reported in step-3 of Scheme2 gave after workup and purification by flash column chromatography[silica gel with dichloromethane/methanol (1:0 to 19:1) to give1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-fluoro-1H-indazole-3-carboxamide(343b) (25 mg, 42%) as a light brown solid; ¹H NMR (300 MHz, DMSO-d₆) δ8.50 (t, J=5.8 Hz, 1H), 7.83-7.75 (m, 2H), 7.72 (dd, J=9.2, 4.2 Hz, 1H),7.51-7.40 (m, 2H), 7.34 (td, J=9.2, 2.5 Hz, 1H), 7.27-7.18 (m, 1H),7.16-7.07 (m, 1H), 5.68 (s, 2H), 4.33 (d, J=5.7 Hz, 2H), 3.98 (s, 2H),3.11-3.01 (m, 1H), 1.04-0.83 (m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−120.96, −121.57; MS (ES+): 498.4 & 500.3 (M+Na); MS (ES−): 510.4(M+Cl).

Preparation of(R)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-5-cyano-1H-indazole-3-carboxamide(344e) Step-1: Preparation of ethyl2-(3-carbamoyl-5-cyano-1H-indazol-1-yl)acetate (344a)

Compound 344a was prepared from ethyl2-(5-bromo-3-carbamoyl-1H-indazol-1-yl)acetate (342a)

(1.0 g, 3.06 mmol) in 1, 4 dioxane (20.0 mL) using zinc cyanide (3.66 g,30.66 mmol), K₂CO₃ (1.05 g, 7.65 mmol) andtetrakis(triphenylphosphine)palladium(0) (1.41 g, 1.226 mmol) accordingto the procedure reported in step-3 of Scheme 301. This gave afterworkup ethyl 2-(3-carbamoyl-5-cyano-1H-indazol-1-yl)acetate (344a)(400.0 mg, 48%) as an off-white solid; ¹H NMR (300 MHz, DMSO-d₆); δ8.628-8.620 (s, 1H), 8.015-7.985 (m, 2H), 7.86-7.83 (d, 1H), 7.657 (s,1H), 5.55 (s, 2H), 4.18-4.16 (m, 2H), 1.23-1.18 (m, 3H); MS (ES−): 271(M−1).

Step-2: Preparation of 2-(3-carbamoyl-5-cyano-1H-indazol-1-yl)aceticacid (344b)

To a stirred solution of ethyl2-(3-carbamoyl-5-cyano-1H-indazol-1-yl)acetate (344a) (400.0 mg, 1.47mmol) in MeOH (20.0 mL,) was added aq. NaOH (0.293 g, 7.30 mmol) andstirred for 12 h at RT. The reaction mixture was concentrated underreduced pressure and aqueous layer was acidified with HCl. The solidobtained was collected by filtration and dried to furnish2-(3-carbamoyl-5-cyano-1H-indazol-1-yl)acetic acid (344b) (200.0 mg,57%) as an off-white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 13.71-13.12 (m,1H), 8.619-8.617 (s, 1H), 8.015-7.95 (m, 2H), 7.849-7.844 (d, 1H), 7.63(s, 1H), 5.50-5.44 (s, 2H); MS (ES−): 243 (M−1).

Step-3: Preparation of(R)-2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)-amino)-N-(3-chloro-2-fluorobenzyl)acetamide(344c)

To a stirred solution of 2-chloro-N-(3-chloro-2-fluorobenzyl) acetamide(35b) (500 mg, 2.13 mmol) in DCM (30 mL) were added(R)-1-((tert-butyldimethylsilyl)oxy)propan-2-amine (314f) (420.0 mg,2.22 mmol) and DIPEA (1.36 mg, 10.54 mmol) at RT. The reaction mixturewas stirred at room temperature for 48 h. The reaction mixture wasconcentrated in vacuum and purified by flash column chromatography[silica gel, eluting with ethyl acetate in n-hexane (0-90%)] to afford(R)-2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)-amino)-N-(3-chloro-2-fluorobenzyl)acetamide(344c) (300.0 mg, 36.34%) as a brown solid; ¹H NMR (300 MHz, DMSO-d₆) δ8.36 (t, J=6.2 Hz, 1H), 7.53-7.38 (m, 1H), 7.32-7.21 (m, 1H), 7.21-7.10(m, 1H), 4.35 (d, J=6.0 Hz, 2H), 3.46-3.31 (m, 2H), 3.18 (d, J=5.5 Hz,2H), 2.67-2.55 (m, 1H), 0.90 (dd, J=6.4, 1.1 Hz, 3H), 0.84 (s, 9H), 0.00(s, 6H); MS (ES+): 389.0 (M+1).

Step-4: Preparation of(R)-1-(2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-5-cyano-1H-indazole-3-carboxamide(344d)

Compound 344d was prepared from(R)-2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)-amino)-N-(3-chloro-2-fluorobenzyl)acetamide(344c) (382 mg, 0.98 mmol) by reaction with2-(3-carbamoyl-5-cyano-1H-indazol-1-yl)acetic acid (344b) (200 mg, 0.82mmol) according to the procedure reported in step-3 of Scheme 2. Thisgave after workup and purification by flash column chromatography[Silica gel, eluting with methanol in ethyl acetate from 0-10%](R)-1-(2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-5-cyano-1H-indazole-3-carboxamide(344d) (400.0 mg, 20%) as an off-white solid.

Step-5: Preparation of(R)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxo ethyl)(1-hydroxypropan-2-yl)amino)-2-oxo ethyl)-5-cyano-1H-indazole-3-carboxamide (344e)

Compound 344e was prepared from(R)-1-(2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-5-cyano-1H-indazole-3-carboxamide(344d) (100 mg, 0.162 mmol) by reaction with ethanolic HCl (10.0 mL) inethanol (10 mL) according to the procedure reported in step-3 of Scheme292. This gave after workup and purification by flash columnchromatography [Silica gel, 24 g eluting with methanol in ethyl acetatefrom 0-5%)(R)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-5-cyano-1H-indazole-3-carboxamide(344e) (60.0 mg, 74%) as an off-white solid; ¹H NMR (300 MHz, DMSO-d₆)(mixture of rotamers) δ 8.90 (t) and 8.67-8.55 (m) (2H), 7.96 (s, 1H),7.86-7.69 (m, 2H), 7.61 (s, 1H), 7.55-7.12 (m, 2H), 6.99 (td, J=7.9, 1.0Hz, 1H), 5.83-5.38 (m) and 4.89-4.71 (m) (3H), 4.51-3.72 (m, 5H),3.54-3.37 (m, 2H), 1.16 (d, J=6.5 Hz) and 0.95 (d, J=6.9 Hz) (2d, 3H);¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.26, −121.60; MS (ES+): 501.4 & 503.4(M+1); MS (ES−): 499.4 & 501.4 (M−1).

Preparation of(R)-tert-butyl(3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazol-5-yl)carbamate(345e) Step-1: Preparation of ethyl2-(5-amino-3-carbamoyl-1H-indazol-1-yl)acetate (345a)

Compound 345a was prepared from ethyl2-(3-carbamoyl-5-nitro-1H-indazol-1-yl)acetate (267c)

(2.0 g, 6.84 mmol) according to the procedure reported in Scheme 313.This gave after workup ethyl2-(5-amino-3-carbamoyl-1H-indazol-1-yl)acetate (345a) (1.795 g) as abrown solid; MS (ES+): 263.3 (M+1).

Step-2: Preparation of ethyl2-(5-((tert-butoxycarbonyl)amino)-3-carbamoyl-1H-indazol-1-yl)acetate(345b)

To a stirred solution of ethyl2-(5-amino-3-carbamoyl-1H-indazol-1-yl)acetate (345a) (3.0 g, 11.45mmol) in DMF (15.0 mL) was added DIPEA (2.7 g, 20.86 mmol) and Bocanhydride (2.7 g, 12.37 mmol) and stirred at RT overnight. Water (50.0mL) was poured into reaction mixture and extracted with EtOAc (3×50.0mL). The combined organic layers were washed with brine, dried andconcentrated under reduced pressure. The crude was purified by flashcolumn chromatography [silica gel, eluting with ethyl acetate inn-hexane (0-50%)] to afford ethyl 2-(5-((tert-butoxycarbonyl)amino)-3-carbamoyl-1H-indazol-1-yl)acetate (345b) (1.3g, 31.3%)as a white solid. Mass: MS (ES+): 363.0 (M+1); MS (ES−): 362.3 (M−1).

Step-3: Preparation of2-(5-((tert-butoxycarbonyl)amino)-3-carbamoyl-1H-indazol-1-yl)aceticacid (345c)

Compound 345c was prepared from ethyl2-(5-((tert-butoxycarbonyl)amino)-3-carbamoyl-1H-indazol-1-yl)acetate(345b) (2.1 g, 5.8 mmol) according to the procedure reported in step-2of Scheme 129. This gave after workup2-(5-(tert-butoxycarbonylamino)-3-carbamoyl-1H-indazol-1-yl)acetic acid(345c) (1.68 g) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ 13.17 (s,1H), 9.37 (s, 1H), 8.38 (s, 1H), 7.64-7.54 (m, 2H), 7.46-7.38 (m, 1H),7.31 (s, 1H), 5.28 (s, 2H), 1.49 (s, 9H); MS (ES+): 357.2 (M+Na).

Step-4: Preparation of (R)-tert-butyl(1-(2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-3-carbamoyl-1H-indazol-5-yl)carbamate(345d)

Compound 345d was prepared from(R)-2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)-amino)-N-(3-chloro-2-fluorobenzyl)acetamide(344c) (174 mg, 0.45 mmol) by reaction with2-(5-((tert-butoxycarbonyl)amino)-3-carbamoyl-1H-indazol-1-yl)aceticacid (345c) (150 mg, 0.45 mmol) according to the procedure reported instep-3 of Scheme 2. This gave after workup and purification by flashcolumn chromatography [Silica gel, eluting with ethyl acetate inn-hexane (0-90%)] (R)-tert-butyl(1-(2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-3-carbamoyl-1H-indazol-5-yl)carbamate(345d) (30 mg, 10%) as a white solid; MS (ES+): 704.0 (M+1): 705; MS(ES−): 703.3 (M−1).

Step-5: Preparation of (R)-tert-butyl(3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazol-5-yl)carbamate (345e)

Compound 345e was prepared from (R)-tert-butyl(1-(2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-3-carbamoyl-1H-indazol-5-yl)carbamate(345d) (100 mg, 0.141 mmol) by reaction with ethanolic HCl (2 drops) indiethyl ether (10 mL) for 1 h. according to the procedure reported instep-3 of Scheme 292. This gave after workup (R)-tert-butyl(3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazol-5-yl)carbamate (345e) (30.0mg, 36%) as an off-white solid; ¹H NMR (300 MHz, DMSO-d₆) (a mixture ofrotamers) δ 9.38 (s, 1H), 8.87 (t) & 8.60 (t, J=5.8 Hz) (2t, 1H), 8.38(s, 1H), 8.01 (s, 1H), 7.60 (s, 1H), 7.56-7.28 (m, 3H), 7.27-7.15 (m,1H), 7.08-6.96 (m, 1H), 5.67-5.25 (m, 2H), 5.48 & 4.80 (t, J=5.7 Hz)(2t, 1H), 4.52-3.71 (m, 5H), 3.52-3.37 (m, 2H), 1.49 (s, 9H), 1.13 (d,J=6.4 Hz) & 0.95 (d, J=7.0 Hz) (2d, 3H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.26, −121.66; MS (ES+): 613.5 & 615.4 (M+Na); MS (ES−): 589.5 (M−1).

Preparation of(R)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-5-(2-cyclopropylacetamido)-1H-indazole-3-carboxamide(346d) Step-1: Preparation of ethyl2-(3-carbamoyl-5-(2-cyclopropylacetamido)-1H-indazol-1-yl)acetate (346a)

Compound 346a was prepared from ethyl2-(5-amino-3-carbamoyl-1H-indazol-1-yl)acetate (345a)

(5.0 g, 19.06 mmol) according to the procedure reported in step-3 ofScheme 2. This gave after workup and purification by flash columnchromatography [silica gel, eluting with ethyl acetate in n-hexane(0-50%)] ethyl2-(3-carbamoyl-5-(2-cyclopropylacetamido)-1H-indazol-1-yl)acetate (346a)(1.0 gm, 15.23%) as a white solid; MS (ES+): 344.0 (M+1), MS (ES−):343.0.0 (M−1).

Step-2: Preparation of2-(3-carbamoyl-5-(2-cyclopropylacetamido)-1H-indazol-1-yl)acetic acid(346b)

Compound 346b was prepared from according to the procedure reported instep-2 of Scheme 344. This gave after workup and purification by flashcolumn chromatography [silica gel, eluting with MeOH in EtOAc (0-10%)]2-(3-carbamoyl-5-(2-cyclopropylacetamido)-1H-indazol-1-yl)acetic acid(346b) (240.0 mg, 65%) as an off-white solid; ¹H NMR (300 MHz, DMSO-d₆)δ 10.14 (s, 1H), 8.04-8.03 (d, 1H), 7.97 (s, 2H), 6.93 (s, 2H),6.74-6.73 (d, 1H), 4.97-4.80 (m, 1H), 4.12-4.10 (m, 2H), 2.0-1.87 (m,4H); MS (ES−): 315.0 (M−1).

Step-3: Preparation of(R)-1-(2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-5-(2-cyclopropylacetamido)-1H-indazole-3-carboxamide(346c)

Compound 346c was prepared from(R)-2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)-amino)-N-(3-chloro-2-fluorobenzyl)acetamide(344c) (122 mg, 0.314 mmol) by reaction with2-(3-carbamoyl-5-(2-cyclopropylacetamido)-1H-indazol-1-yl)acetic acid(346b) (100 mg, 0.32 mmol) according to the procedure reported in step-3of Scheme 2. This gave after workup and purification by flash columnchromatography [Silica gel, eluting with ethyl acetate in n-hexane(0-90%)](R)-1-(2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-5-(2-cyclopropylacetamido)-1H-indazole-3-carboxamide(346c) (70.0 mg, 32%) as a light brown solid; MS (ES−): 685 (M−1).

Step-4: Preparation of(R)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-5-(2-cyclopropylacetamido)-1H-indazole-3-carboxamide(346d)

Compound 346d was prepared from(R)-1-(2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-5-(2-cyclopropylacetamido)-1H-indazole-3-carboxamide(346c) (160 mg, 0.232 mmol) by reaction with ethanolic HCl (8 mL) inethanol (10 mL) according to the procedure reported in step-3 of Scheme292. This gave after workup(R)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-5-(2-cyclopropylacetamido)-1H-indazole-3-carboxamide(346d) (17.0 mg, 13%) as a white solid; MS (ES+): 573 (M+1), MS (ES−):571 (M−1).

Preparation of1-(2-(((trans)-3-aminocyclobutyl)(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-5-nitro-1H-indazole-3-carboxamide(347b) Step-1: Preparation of tert-butyl((trans)-3-(2-(3-carbamoyl-5-nitro-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)acetamido)cyclobutyl)carbamate(347a)

Reaction of tert-butyl((trans)-3-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)cyclobutyl)carbamate(169a) (570 mg, 1.48 mmol) with2-(3-carbamoyl-5-nitro-1H-indazol-1-yl)acetic acid (267d) (300 mg, 1.14mmol) according to the procedure reported in step-3 of Scheme 2 gaveafter workup and purification by flash column chromatography [Silicagel, (12 g) eluting with EtOAc in DCM 0 to 100% as eluents] tert-butyl((trans)-3-(2-(3-carbamoyl-5-nitro-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)acetamido)cyclobutyl)carbamate(347a) (0.52 g, 73% yield) as a white powder; ¹H NMR (300 MHz, DMSO-d₆)(a mixture of two rotamers) δ 9.06 and 9.05 (2s, 1H), 8.89 and 8.44 (2t,J=5.9 Hz, 1H), 8.33-8.22 (m, 1H), 8.03 and 7.69 (2s, 2H), 7.84 and 7.77(2d, J=9.3 Hz, 1H), 7.57-7.29 (m, 2H), 7.26-6.99 (m, 1H), 5.65 and 5.54(2s, 2H), 4.92-4.75 (m, 1H), 4.47 and 4.32 (2d, J=5.8 Hz, 2H), 4.32 and4.04 (2s, 2H), 3.89-3.77 (m, 1H), 2.33-2.11 (m, 4H), 1.40 and 1.36 (2s,9H); MS (ES+): 654.5 and 655.5 (M+Na); (ES−): 630.6 (M−1).

Step-2: Preparation of1-(2-(((trans)-3-aminocyclobutyl)(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-5-nitro-1H-indazole-3-carboxamide(347b)

Reaction of tert-butyl((trans)-3-(2-(3-carbamoyl-5-nitro-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)acetamido)cyclobutyl)carbamate(347a) (0.8 g, 1.266 mmol) with TFA (0.975 mL, 12.66 mmol) according tothe procedure reported in step-2 of Scheme 2 gave after workup andpurification by flash column chromatography [Silica gel, (12 g) elutingwith DMA80 in DCM, 0 to 50% as eluents]1-(2-(((trans)-3-aminocyclobutyl)(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-5-nitro-1H-indazole-3-carboxamide(347b) (0.03 g, 5% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) (amixture of two rotamers) δ 9.058 and 9.05 (2s, 1H), 8.88 and 8.43 (2t,J=5.9 Hz, 1H), 8.31 and 8.25 (2dd, J=9.3, 2.3 Hz, 1H), 8.03 and 8.00(2s, 1H), 7.85 and 7.77 (2d, J=9.3 Hz, 1H), 7.69 (s, 1H), 7.57-6.85 (m,3H), 5.65 and 5.54 (2s, 2H), 4.99-4.83 (m, 1H), 4.47 and 4.32 (2d, J=5.9Hz, 2H), 4.29 and, 4.02 (2s, 2H), 3.48-3.24 (m, 1H), 3.10-2.77 (m, 2H),2.25-2.10 (m, 1H), 2.12-1.90 (m, 2H), 1.87-1.73 (m, 1H); ¹⁹F NMR (282MHz, DMSO-d₆) (a mixture of two rotamers) δ −121.24, −121.59; MS (ES+):532.4 (M+1).

Preparation of1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)-amino)-2-oxoethyl)-6-fluoro-1H-indazole-3-carboxamide(348b)

Reaction of 2-(3-carbamoyl-6-fluoro-1H-indazol-1-yl)acetic acid (348a)(202 mg, 0.853 mmol; prepared according to the procedure reported byAltmann, Eva et al; in PCT Int. Appl., 2014002058, 3 Jan. 2014) withN-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide (10b) (328 mg,1.28 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column chromatography[silica gel with dichloromethane/methanol (1:0 to 19:1) to give1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-6-fluoro-1H-indazole-3-carboxamide(348b) (80 mg, 20%) as a light brown solid; ¹H NMR (300 MHz, DMSO-d₆) δ8.50 (t, J=5.8 Hz, 1H), 8.18 (dd, J=8.9, 5.4 Hz, 1H), 7.78 (s, 1H), 7.56(dd, J=9.8, 2.2 Hz, 1H), 7.52-7.34 (m, 2H), 7.26-7.05 (m, 3H), 5.62 (s,2H), 4.33 (d, J=5.7 Hz, 2H), 3.98 (s, 2H), 3.13-2.98 (m, 1H), 1.05-0.81(m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −114.79, −121.60; MS (ES+): 498.4& 500.4 (M+Na); MS (ES−): 510.4 (M+Cl).

Preparation of1-(2-(((trans)-3-aminocyclobutyl)(2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(349d) Step-1: Preparation of tert-butyl((trans)-3-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)amino)cyclobutyl)carbamate(349b)

To a solution of N-(6-bromopyridin-2-yl)-2-chloroacetamide (349a) (0.55g, 2.204 mmol, prepared according to the procedure reported by Cheriard,Berland L. and Wu, Xinyuan; in PCI Int Appl., 2016044792, 24 Mar. 2016)in THF (10 mL) was added DIPEA (0.578 mL, 3.31 mmol), tert-butyl(trans)-3-aminocyclobutylcarbamate (0.452 g, 2.425 mmol) and stirred at60° C. for 24h. Mixture was poured into sat. NaHCO₃ solution (60 ml) andresultant suspension was extracted with EtOAc (2×80 ml). The combinedorganics were washed with brine, dried, filtered, concentrated andpurified by flash column chromatography [silica gel 24 g, EtOAc inhexanes as eluents 0 to 100%] to afford tert-butyl((trans)-3-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)amino)cyclobutyl)carbamate(349b) (0.43 g, 49% yield) as off-white solid; ¹H NMR (300 MHz, DMSO-d₆)δ 10.45 (s, 1H), 8.10 (dd, J=8.1, 0.7 Hz, 1H), 7.75 (t, J=8.0 Hz, 1H),7.35 (dd, J=7.7, 0.7 Hz, 1H), 7.15 (d, J=7.6 Hz, 1H), 4.09-3.93 (m, 1H),3.27-3.14 (m, 3H), 2.03-1.89 (m, 4H), 1.36 (s, 9H); MS (ES+): 421.3,423.3 (M+Na), MS (ES−): 397.3, 399.3 (M−1).

Step-2: Preparation of tert-butyl((trans)-3-(N-(2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)-2-(3-carbamoyl-1H-indazol-1-yl)acetamido)cyclobutyl)carbamate(349c)

Reaction of tert-butyl((trans)-3-((2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)amino)cyclobutyl)carbamate(349b) (100 mg, 0.25 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (66 mg, 0.30 mmol) according to the procedure reported instep-3 of scheme-2 gave after workup and purification by flash columnchromatography [Silica gel, (4 g) eluting with EtOAc in DCM 0 to 100% aseluents] tert-butyl((trans)-3-(N-(2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)-2-(3-carbamoyl-1H-indazol-1-yl)acetamido)cyclobutyl)carbamate(349c) (0.12 g, 80% yield) as a white powder; ¹H NMR (300 MHz, DMSO-d₆)(a mixture of two rotamers) δ 11.25 and 10.90 (2s, 1H), 8.23-8.11 (m,1H), 8.05-7.91 (m, 1H), 7.87-7.55 (m, 2H), 7.50-7.18 (m, 5H), 5.57 and5.44 (2s, 2H), 4.98-4.81 (m, 1H), 4.55 and 4.22 (2s, 2H), 3.92-3.75 (m,1H), 2.33-2.14 (m, 2H), 2.13-1.97 (m, 2H), 1.39 and 1.34 (2s, 9H).

Step-3: Preparation of1-(2-(((trans)-3-aminocyclobutyl)(2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(349d)

Reaction of tert-butyl((trans)-3-(N-(2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)-2-(3-carbamoyl-1H-indazol-1-yl)acetamido)cyclobutyl)carbamate(349c) (0.12 g, 0.2 mmol) with TFA (0.15 mL, 2.0 mmol) according to theprocedure reported in step-2 of scheme-2 gave after workup andpurification by flash column chromatography [Silica gel, (12 g) elutingwith DMA80 in DCM, 0 to 50% as eluents]1-(2-(((trans)-3-aminocyclobutyl)(2-((6-bromopyridin-2-yl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(349d) (0.075 g, 75% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆)(a mixture of two rotamers) δ 10.88 (s, 1H), 8.23-7.96 (m, 2H),7.87-7.54 (m, 3H), 7.49-7.19 (m, 4H), 5.56 and 5.44 (2s, 2H), 5.03-4.86(m, 1H), 4.53 and 4.21 (2s, 2H), 3.46-3.20 (m, 3H), 2.41-2.31 (m, 1H),2.25-1.95 (m, 2H), 1.86-1.73 (m, 1H); MS (ES+): 500.4, 502.4 (M+1), MS(ES−): 498.4, 500.4 (M−1).

Preparation of1-(2-(((trans)-3-aminocyclobutyl)(2-((6-bromopyrazin-2-yl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(350c) Step-1: Preparation of tert-butyl((trans)-3-((2-((6-bromopyrazin-2-yl)amino)-2-oxoethyl)amino)cyclobutyl)carbamate(350a)

Compound 350a was prepared fromN-(6-bromopyrazin-2-yl)-2-chloroacetamide (49b) (0.5 g, 1.4 mmol)according to the procedure reported in step-1 of scheme-349. This gaveafter workup and purification by flash column chromatography [silica gel24 g, EtOAc in hexanes as eluents 0 to 100%] tert-butyl((trans)-3-((2-((6-bromopyrazin-2-yl)amino)-2-oxoethyl)amino)cyclobutyl)carbamate(350a) (0.08 g, 14% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) δ9.32 (d, J=0.6 Hz, 1H), 8.56 (d, J=0.6 Hz, 1H), 7.14 (d, J=7.6 Hz, 1H),4.07-3.95 (m, 1H), 3.31-3.14 (m, 3H), 1.96 (t, J=6.5 Hz, 4H), 1.36 (s,9H); MS (ES+): 400.4, 402.4 (M, M+2), 422.3, 424.4 (M+Na).

Step-2: Preparation of tert-butyl((trans)-3-(N-(2-((6-bromopyrazin-2-yl)amino)-2-oxoethyl)-2-(3-carbamoyl-1H-indazol-1-yl)acetamido)cyclobutyl)carbamate(350b)

Reaction of tert-butyl((trans)-3-((2-((6-bromopyrazin-2-yl)amino)-2-oxoethyl)amino)cyclobutyl)carbamate(350a)(80 mg, 0.2 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)acetic acid(2e) (53 mg, 0.24 mmol) according to the procedure reported in step-3 ofscheme-2 gave after workup and purification by flash columnchromatography [Silica gel, (4 g) eluting with DMA80 in DCM 0 to 30% aseluents] tert-butyl((trans)-3-(N-(2-((6-bromopyrazin-2-yl)amino)-2-oxoethyl)-2-(3-carbamoyl-1H-indazol-1-yl)acetamido)cyclobutyl)carbamate(350b) (0.09 g, 75% yield) as a white solid; MS (ES+): 601.4, 603.4 (M,M+2).

Step-3: Preparation of1-(2-(((trans)-3-aminocyclobutyl)(2-((6-bromopyrazin-2-yl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(350c)

Reaction of tert-butyl((trans)-3-(N-(2-((6-bromopyrazin-2-yl)amino)-2-oxoethyl)-2-(3-carbamoyl-1H-indazol-1-yl)acetamido)cyclobutyl)carbamate(350b) (0.09 g, 0.15 mmol) with TFA (0.23 mL, 3.0 mmol) according to theprocedure reported in step-2 of scheme-2 gave after workup andpurification by flash column chromatography [Silica gel, (12 g) elutingwith DMA80 in DCM, 0 to 50% as eluents]1-(2-(((trans)-3-aminocyclobutyl)(2-((6-bromopyrazin-2-yl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(350c) (0.06 g, 80% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆)(a mixture of two rotamers) δ 9.38 and 9.24 (2s, 1H), 8.62 and 8.54 (2s,1H), 8.21-8.13 (m, 1H), 7.71 (s, 1H), 7.62 and 7.60 (2d, J=3.4 Hz, 1H),7.49-7.35 (m, 3H), 7.31-7.20 (m, 1H), 5.57 and 5.45 (2s, 2H), 4.96 (q,J=7.9 Hz, 1H), 4.55 and 4.25 (2s, 2H), 3.49-3.22 (m, 1H), 2.45-1.97 (m,3H), 1.94-1.76 (m, 1H); MS (ES+): 501.2, 503.2 (M, M+2), 523.2, 525.2(M+Na).

Preparation of5-amino-1-(2-(((trans)-3-aminocyclobutyl)(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(351b) Step-1: Preparation of tert-butyl((trans)-3-(2-(5-amino-3-carbamoyl-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)acetamido)cyclobutyl)carbamate(351a)

Compound 351a was prepared from tert-butyl((trans)-3-(2-(3-carbamoyl-5-nitro-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)acetamido)cyclobutyl)carbamate(347a)

(0.4 g, 0.63 mmol) according to the procedure reported in step-6 ofScheme 328. This gave after workup and purification by flashchromatography [silica gel 12 g, DMA80 in DCM 0 to 30% as eluents]tert-butyl((trans)-3-(2-(5-amino-3-carbamoyl-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)acetamido)cyclobutyl)carbamate(351a) (0.25 g, 66% yield) as a off-white solid; MS (ES+): 602.5 (M+1),MS (ES−): 636.5 (M+Cl).

Step-2: Preparation of5-amino-1-(2-(((trans)-3-aminocyclobutyl)(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(351b)

Compound 351b was prepared from tert-butyl((trans)-3-(2-(5-amino-3-carbamoyl-1H-indazol-1-yl)-N-(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)acetamido)cyclobutyl)carbamate(351a) (0.08 g, 0.133 mmol) using TFA (0.205 mL, 2.66 mmol) according tothe procedure reported in step-2 of Scheme 2. This gave after workup andpurification by flash column chromatography [Silica gel, (4 g) elutingwith DMA80 in DCM, 0 to 50% as eluents]5-amino-1-(2-(((trans)-3-aminocyclobutyl)(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(351b) (0.053 g, 79% yield) as a white solid; ¹H NMR (300 MHz, DMSO-d₆)δ 8.89 and 8.51 (2t, J=6.0 Hz, 1H), 8.10 and 8.01 (2s, 2H), 7.64-6.88(m, 9H), 5.43 and 5.30 (2s, 2H), 5.14-4.91 (m, 1H), 4.46 (d, J=5.6 Hz,1H), 4.36-4.28 (m, 2H), 4.05 (s, 1H), 3.74-3.15 (m, 2H), 2.68-2.58 and2.46-2.30 (2m, 2H), 2.23-2.09 (m, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) (amixture of two rotamers) δ −121.25, −121.59; MS (ES+) 502.4 (M+1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(hydroxymethyl)-1H-indazole-3-carboxamide(352b) Step 1 Preparation of3-carbamoyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylic(ethyl carbonic) anhydride (352a)

To a suspension of3-carbamoyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylicacid (199a) (100 mg, 0.199 mmol) in DCM (2 mL) was added triethylamine(0.083 mL, 0.598 mmol) followed by ethyl carbonochloridate (0.029 mL,0.299 mmol) at 0° C. The reaction mixture was stirred at 0° C. anddiluted with dichloromethane (100 mL). The reaction mixture was washedwith water (50 mL) and brine (50 mL), dried, filtered and concentratedin vacuum to afford3-carbamoyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylic(ethyl carbonic) anhydride (352a) (108 mg) as an off-white solid, whichwas used as such for next step.

Step 2 Preparation of1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(hydroxymethyl)-1H-indazole-3-carboxamide(352b)

To a solution of3-carbamoyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-5-carboxylic(ethyl carbonic) anhydride (352a) (the above crude product, 93 mg, 0.162mmol) in methanol (4 mL) was added sodium borohydride (12.51 mg, 0.324mmol) and stirred at RT for 0.5 h. The reaction mixture was diluted withethyl acetate (80 mL), neutralized with acetic acid, washed with water(40 mL), brine (40 mL), dried, filtered and concentrated in vacuum. Thecrude product was purified by flash column chromatography [silica gel,eluting with hexanes/10% methanol in ethyl acetate (1:0 to 0:1)] toafford1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-5-(hydroxymethyl)-1H-indazole-3-carboxamide(352b) (17 mg, 20% for two steps) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 8.50 (t, J=5.9 Hz, 1H), 8.14 (s, 1H), 7.69 (s, 1H), 7.58 (d,J=8.8 Hz, 1H), 7.50-7.42 (m, 1H), 7.40-7.31 (m, 2H), 7.26-7.18 (m, 1H),7.12 (t, J=7.8 Hz, 1H), 5.64 (s, 2H), 5.27 (t, J=5.7 Hz, 1H), 4.61 (d,J=5.6 Hz, 2H), 4.33 (d, J=5.6 Hz, 2H), 3.98 (s, 2H), 3.16-2.94 (m, 1H),1.10-0.79 (m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.60; MS (ES+): 510.4& 512.4 (M+Na); MS (ES−): 486.4 (M−1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-6-(hydroxymethyl)-1H-indazole-3-carboxamide(353b) Step 1 Preparation of3-carbamoyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-6-carboxylic(ethyl carbonic) anhydride (353a)

Reaction of3-carbamoyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-6-carboxylicacid (208a) (100 mg, 0.199 mmol) with ethyl carbonochloridate (0.029 mL,0.299 mmol according to the procedure reported in step-1 of Scheme 352gave after workup3-carbamoyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-6-carboxylic(ethyl carbonic) anhydride (353a) (107 mg) as a white solid, which wasused as such for next step; MS (ES+): 510.4 & 596.4 (M+Na).

Step 2 Preparation of1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-6-(hydroxymethyl)-1H-indazole-3-carboxamide(353b)

Reaction of3-carbamoyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-6-carboxylic(ethyl carbonic) anhydride (353a) (97 mg, 0.169 mmol, crude) with sodiumborohydride (13.05 mg, 0.338 mmol) according to the procedure reportedin step-2 of Scheme 352 gave after workup and purification by flashcolumn chromatography [silica gel with dichloromethane/methanol (1:0 to19:1)]1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-6-(hydroxymethyl)-1H-indazole-3-carboxamideas a white solid (353b) (28 mg, 32% for two steps). ¹H NMR (300 MHz,DMSO-d₆) δ 8.51 (t, J=5.9 Hz, 1H), 8.10 (d, J=8.4 Hz, 1H), 7.70 (s, 1H),7.57 (s, 1H), 7.50-7.41 (m, 1H), 7.36 (s, 1H), 7.28-7.18 (m, 2H), 7.12(t, J=7.8 Hz, 1H), 5.64 (s, 2H), 5.36 (t, J=5.6 Hz, 1H), 4.62 (d, J=5.6Hz, 2H), 4.33 (d, J=5.7 Hz, 2H), 3.99 (s, 2H), 3.12-2.98 (m, 1H),1.04-0.87 (m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.60; MS (ES+): 510.4& 512.4 (M+Na); MS (ES−): 522.5 (M+Cl).

Preparation of6-chloro-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(354b)

Reaction of 2-(3-carbamoyl-6-chloro-1H-indazol-1-yl)acetic acid (300 mg,1.183 mmol), prepared according to the procedure reported by Altmann;Eva et al; in PCI int. Appl 2014002058, 3 Jan. 2014), withN-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide (10b) (455 mg,1.774 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column chromatography byflash column chromatography [silica gel with hexanes/10% methanol inethyl acetate (1:0 to 1:1)]6-chloro-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)-(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(108 mg, 19%) as a light brown solid. ¹H NMR (300 MHz, DMSO-d₆) δ 8.51(t, J=5.8 Hz, 1H), 8.17 (dd, J=8.7, 0.7 Hz, 1H), 7.90 (dd, J=1.8, 0.7Hz, 1H), 7.82 (s, 1H), 7.51-7.42 (m, 2H), 7.28 (dd, J=8.7, 1.7 Hz, 1H),7.26-7.19 (m, 1H), 7.14-7.07 (m, 1H), 5.66 (s, 2H), 4.33 (d, J=5.7 Hz,2H), 3.98 (s, 2H), 3.17-2.94 (m, 1H), 1.05-0.84 (m, 4H); ¹⁹F NMR (282MHz, DMSO-d₆) δ −121.62; MS (ES+): 514.4 & 516.4 (M+Na); MS (ES−): 490.4(M−1).

Preparation of6-acetyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)(cyclopropyl)-amino)-2-oxo-ethyl)-1H-indazole-3-carboxamide(355f) Step 1: Preparation of 6-bromo-1H-indazole-3-carboxamide (355b)

To a solution of 6-bromo-1H-indazole-3-carboxylic acid (355a) (2 g, 8.30mmol) in THF (40 mL) at −15° C. was added isobutyl chloroformate (1.77mL, 13.28 mmol) and 4-methylmorpholine (1.47 mL, 13.28 mmol) and stirredat −15° C. for 2 h. The reaction mixture was treated with conc. ammoniumhydroxide (5.61 mL, 83 mmol) at −15° C., stirred at −15° C. for 1 h andallowed to warm to RT overnight. The reaction mixture was diluted withethyl acetate (200 mL) and water (100 mL). The solid obtained wascollected by filtration dried in vacuum to afford6-bromo-1H-indazole-3-carboxamide (355b) (1.148 g, 58%) as a lightyellow solid; ¹H NMR (300 MHz, DMSO-d₆) δ 13.52 (s, 1H), 8.10 (d, J=8.6Hz, 1H), 7.88-7.80 (m, 2H), 7.43 (s, 1H), 7.39-7.33 (m, 1H).

Step 2: Preparation of ethyl2-(6-bromo-3-carbamoyl-1H-indazol-1-yl)acetate (355c)

Reaction of 6-bromo-1H-indazole-3-carboxamide (355b) (1.1 g, 4.58 mmol)with ethylbromoacetate (0.73 mL, 6.42 mmol) according to the procedurereported in step-1 of Scheme 43 gave after workup ethyl2-(6-bromo-3-carbamoyl-1H-indazol-1-yl)acetate (355c) (1.403 g, 94%yield) as an off-white solid, which was used as such for next step; MS(ES+): 348.2, 350.2 (M+Na).

Step 3: Preparation of ethyl2-(6-acetyl-3-carbamoyl-1H-indazol-1-yl)acetate (355d)

Reaction of ethyl 2-(6-bromo-3-carbamoyl-1H-indazol-1-yl)acetate (355c)(300 mg, 0.92 mmol) with tributyl(1-ethoxyvinyl)stannane (0.4 mL, 1.15mmol) according to the procedure reported in step-1 and step-2 of Scheme206 gave after workup and purification by flash column chromatography[silica gel with hexanes/10% methanol in ethyl acetate (1:0 to 1:1)]ethyl 2-(6-acetyl-3-carbamoyl-1H-indazol-1-yl)acetate as a white solid(355d) 126 mg, 45% for two steps) as a light yellow solid; ¹H NMR (300MHz, DMSO-d₆) δ 8.53-8.51 (m, 1H), 8.27 (dd, J=8.6, 0.8 Hz, 1H),7.87-7.80 (m, 2H), 7.54 (s, 1H), 5.61 (s, 2H), 4.18 (q, J=7.1 Hz, 2H),2.68 (s, 3H), 1.22 (t, J=7.1 Hz, 3H); MS (ES+): 312.4 (M+Na).

Step 4: Preparation of 2-(6-acetyl-3-carbamoyl-1H-indazol-1-yl)aceticacid (355e)

Reaction of ethyl 2-(6-acetyl-3-carbamoyl-1H-indazol-1-yl)acetate (355d)(109 mg, 0.38 mmol) with lithium hydroxide hydrate (97.0 mg, 2.26 mmol)according to the procedure reported in step-2 of Scheme 129 gave afterworkup and purification 2-(6-acetyl-3-carbamoyl-1H-indazol-1-yl)aceticacid (355e) (75 mg, 76%) (75 mg, 76%) as a yellow solid; ¹H NMR (300MHz, DMSO-d₆) δ 13.36 (s, 1H), 8.51 (t, J=1.1 Hz, 1H), 8.26 (dd, J=8.6,0.8 Hz, 1H), 7.89-7.76 (m, 2H), 7.52 (s, 1H), 5.49 (s, 2H), 2.68 (s,3H); MS (ES−): 260.4 (M−1).

Step 5: Preparation of6-acetyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)-(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(355f)

Reaction of 2-(6-acetyl-3-carbamoyl-1H-indazol-1-yl)acetic acid (355e)(45 mg, 0.172 mmol) withN-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide (10b) (66 mg,0.26 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column chromatography[silica gel with dichloromethane/methanol (1:0 to 19:1)]6-acetyl-1-(2-((2-(3-chloro-2-fluorobenzylamino)-2-oxoethyl)-(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(355f) (28 mg, 33%) as a light brown solid; ¹H NMR (300 MHz, DMSO-d₆) δ8.54 (t, J=5.8 Hz, 1H), 8.35-8.33 (m, 1H), 8.26 (dd, J=8.6, 0.8 Hz, 1H),7.84 (s, 1H), 7.82 (dd, J=8.6, 1.3 Hz, 1H), 7.49 (s, 1H), 7.47-7.39 (m,1H), 7.24-7.16 (m, 1H), 7.05 (td, J=7.8, 1.1 Hz, 1H), 5.79 (s, 2H), 4.33(d, J=5.7 Hz, 2H), 4.00 (s, 2H), 3.16-3.01 (m, 1H), 2.64 (s, 3H),1.05-0.88 (m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.63; MS (ES+): 522.4(M+Na); MS (ES−): 498.6 (M−1), 534.4 & 536.5 (M+Cl).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-6-cyano-1H-indazole-3-carboxamide(356c) Step 1: Preparation of ethyl2-(3-carbamoyl-6-cyano-1H-indazol-1-yl)acetate (356a)

Compound 356a was prepared from ethyl2-(6-bromo-3-carbamoyl-1H-indazol-1-yl)acetate (355c) (300 mg, 0.92mmol) in 1, 4 dioxane (10.0 mL) using zinc cyanide (1.08 g, 9.2 mmol),K₂CO₃ (321 mg, 2.3 mmol) and tetrakis(triphenylphosphine)palladium(0)(425 mg, 0.368 mmol) according to the procedure reported in step-3 ofScheme 301. This gave after workup and purification by flash columnchromatography [silica gel, eluting with hexanes/10% methanol in ethylacetate (1:0 to 0:1)] to give ethyl2-(3-carbamoyl-6-cyano-1H-indazol-1-yl)acetate (356a) (23 mg) as a whitesolid, which was used as such for next step. MS (ES−): 271.4 (M−1).

Step 2: Preparation of 2-(3-carbamoyl-6-cyano-1H-indazol-1-yl)aceticacid (356b)

Reaction of ethyl 2-(3-carbamoyl-6-cyano-1H-indazol-1-yl)acetate (356a)(20 mg, 0.073 mmol) with lithium hydroxide hydrate (19 mg, 0.44 mmol)according to the procedure reported in step-2 of Scheme 129 gave afterworkup 2-(3-carbamoyl-6-cyano-1H-indazol-1-yl)acetic acid (356b) (10 mg,5% for 3 steps) as a white solid; MS (ES−): 243.4 (M−1).

Step 3: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-6-cyano-1H-indazole-3-carboxamide(356c)

Reaction of 2-(3-carbamoyl-6-cyano-1H-indazol-1-yl)acetic acid (356b)(10 mg, 0.041 mmol) withN-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide (10b) (16 mg,0.06 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column chromatography[silica gel with dichloromethane/methanol (1:0 to 19:1)]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-6-cyano-1H-indazole-3-carboxamide(356c) (6 mg, 30%) as a light yellow solid; ¹H NMR (300 MHz, DMSO-d₆) δ8.51 (t, J=5.8 Hz, 1H), 8.43 (t, J=1.1 Hz, 1H), 8.36-8.30 (m, 1H), 7.92(s, 1H), 7.59 (dd, J=8.5, 1.3 Hz, 1H), 7.56 (s, 1H), 7.48-7.42 (m, 1H),7.25-7.18 (m, 1H), 7.12-7.04 (m, 1H), 5.74 (s, 2H), 4.33 (d, J=5.8 Hz,2H), 3.99 (s, 2H), 3.07 (s, 1H), 1.08-0.83 (m, 4H); ¹⁹F NMR (282 MHz,DMSO-d₆) δ −121.59; MS (ES+): 505.4 & 507.5 (M+Na).

Preparation of(R)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3,5-dicarboxamide(357a)

Reaction of(R)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-5-cyano-1H-indazole-3-carboxamide(344e) (17 mg, 0.034 mmol) with hydrogen peroxide (0.012 mL, 0.136 mmol)according to the procedure reported in Scheme 65 gave after workup andpurification by flash column chromatography on silica gel withdichloromethane/methanol (1:0 to 4:1) to give(R)-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3,5-dicarboxamide(357a) (5 mg, 28%). ¹H NMR (300 MHz, DMSO-d₆, a mixture of two rotamers)δ 8.97-8.53 (m, 2H), 8.10 (s, 1H), 7.90 (t, J=9.5 Hz, 1H), 7.79 (s, 1H),7.60-6.94 (m, 6H), 5.80-5.41 (m, 3H), 4.90-3.60 (m, 5H), 3.60-3.10 (m,2H), 1.15 (d, J=6.5 Hz) and 0.96 (d, J=6.7 Hz) (2d, 3H); ¹⁹F NMR (282MHz, DMSO-d₆) δ −121.27, −121.64; MS (ES+): 541.4 & 543.4 (M+Na).

Preparation of5-amino-1-(2-((2-(((S)-1-(3-chloro-2-fluorophenyl)-3-(dimethylamino)propyl)amino)-2-oxoethyl)((R)-1-hydroxypropan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(358j) Step-1: Preparation of (5)-tert-butyl3-(3-chloro-2-fluorophenyl)-3-((R)-1,1-dimethylethyl-sulfinamido)propanoate(358b)

To a solution of(R,E)-N-(3-chloro-2-fluorobenzylidene)-2-methylpropane-2-sulfinamide(358a) (500 mg, 1.91 mmol; prepared according to the procedure reportedby Lam, Patrick Y. S. et al; in PCI′ flat. Appl., 2013022814, 14 Feb.2013) in THF (12 mL) cooled with ice/water was added dropwise(2-tert-butoxy-2-oxoethyl)zinc(II) chloride (9.93 mL, 4.97 mmol) andstirred at 0° C. for 2 h. The reaction mixture was allowed to warm to RTover a period of 2 h, quenched with sat. NH₄Cl (50 mL), water (50 mL)and extracted with ethyl acetate (120 mL). The organic layer wasseparated washed with brine (60 mL), dried filtered and concentrated togive (5)-tert-butyl3-(3-chloro-2-fluorophenyl)-3-((R)-1,1-dimethylethylsulfinamido)propanoate(358b) (775 mg) as a light yellow oil which was used as such for nextstep. MS (ES+): 400.4 & 402.4 (M+Na).

Step-2: Preparation of(R)—N—((S)-1-(3-chloro-2-fluorophenyl)-3-hydroxypropyl)-2-methylpropane-2-sulfinamide(358c)

To a solution of (S)-tert-butyl3-(3-chloro-2-fluorophenyl)-3-((R)-1,1-dimethylethylsulfinamido)propanoate(358b) (600 mg, 1.59 mmol) in THF (9 mL) was added lithium borohydride(1.588 mL, 3.18 mmol, 2M in THF), MeOH (0.4 mL) and stirred at RT for28.5 h. The reaction mixture was quenched with sat. NH₄Cl (20 mL), water(50 mL) and extracted with ethyl acetate (120 mL). The organic layer waswashed with brine (60 mL), dried filtered, concentrated in vacuum andpurified by flash column chromatography [silica gel, eluting withdichloromethane/methanol (1:0 to 19:1)] to give(R)—N—((S)-1-(3-chloro-2-fluorophenyl)-3-hydroxypropyl)-2-methylpropane-2-sulfinamide(358c) (133 mg, 27% for 2 steps) as a white solid; ¹H NMR (300 MHz,DMSO-d₆) δ 7.53-7.38 (m, 2H), 7.23 (td, J=7.9, 1.1 Hz, 1H), 5.72 (d,J=5.7 Hz, 1H), 4.78-4.64 (m, 2H), 3.60-3.44 (m, 1H), 3.46-3.28 (m, 1H),2.11-1.96 (m, 1H), 1.91-1.73 (m, 1H), 1.05 (d, J=1.4 Hz, 9H); ¹⁹F NMR(282 MHz, DMSO-d₆) δ −122.03; MS (ES+): 330.3 (M+Na).

Step-3: Preparation of(S)-3-(3-chloro-2-fluorophenyl)-3-((R)-1,1-dimethylethyl-sulfinamido)propylmethanesulfonate (358d)

To a solution of(R)—N—((S)-1-(3-chloro-2-fluorophenyl)-3-hydroxypropyl)-2-methylpropane-2-sulfinamide(358c) (162 mg, 0.526 mmol) and triethylamine (0.147 mL, 1.053 mmol) inCH₂C₁₂ (4 mL) was cooled to ˜−10° C. was added methanesulfonyl chloride(0.045 mL, 0.579 mmol) and stirred at ˜0° C. for 1.5 h. The reactionmixture was diluted with dichloromethane (75 mL), and (40 mL) at ˜0° C.The organic layer was separated dried, filtered and concentrated invacuum to give(S)-3-(3-chloro-2-fluorophenyl)-3-((R)-1,1-dimethylethyl-sulfinamido)propylmethanesulfonate (358d) (214 mg) as a colorless gum; MS (ES+): 408.3 &410.2 (M+Na).

Step-4: Preparation of(R)—N—((S)-1-(3-chloro-2-fluorophenyl)-3-(dimethylamino)propyl)-2-methylpropane-2-sulfinamide(358e)

To a solution of(S)-3-(3-chloro-2-fluorophenyl)-3-((R)-1,1-dimethylethylsulfinamido)propylmethanesulfonate (358d) (0.095 g, 0.246 mmol) in ethanol (5 mL) wasadded dimethylamine (2M in THF, 2.71 mL, 5.41 mmol) and stirred at 80°C. in a sealed container for 2 h. The reaction mixture was cooled to RTand concentrated to dryness to give(R)—N—((S)-1-(3-chloro-2-fluorophenyl)-3-(dimethylamino)propyl)-2-methylpropane-2-sulfinamide(358e) (121 mg) as a yellow gum; MS (ES+): 357.4 & 359.4 (M+Na).

Step-5: Preparation of(S)-1-(3-chloro-2-fluorophenyl)-N3,N3-dimethylpropane-1,3-diamine (358f)

To a solution of(R)—N—((S)-1-(3-chloro-2-fluorophenyl)-3-(dimethylamino)propyl)-2-methylpropane-2-sulfinamide(358e) (0.076 g, 0.228 mmol) in MeOH (4 mL) was added hydrogen chloride(0.114 mL, 0.456 mmol, 4 N in 1,4-dioxane) and stirred at RT for 5 h.The reaction mixture was concentrated in vacuum to give(S)-1-(3-chloro-2-fluorophenyl)-N3,N3-dimethylpropane-1,3-diamine (358f)(105 mg) as a yellow gum; MS (ES+): 231.4 & 233.3 (M+Na).

Step-6: Preparation of (R)-ethyl2-(2-(5-(tert-butoxycarbonylamino)-3-carbamoyl-1H-indazol-1-yl)-N-(1-(tert-butyldimethylsilyloxy)propan-2-yl)acetamido)acetate(358g)

Reaction of2-(5-((tert-butoxycarbonyl)amino)-3-carbamoyl-1H-indazol-1-yl)aceticacid (345c) (200 mg, 0.598 mmol) with (R)-ethyl2-(1-(tert-butyldimethylsilyloxy)propan-2-ylamino)acetate (329a) (198mg, 0.718 mmol) according to the procedure reported in step-3 of Scheme2 gave after workup and purification by flash column chromatography[silica gel with dichloromethane/methanol (1:0 to 19:1)] (R)-ethyl2-(2-(5-(tert-butoxycarbonylamino)-3-carbamoyl-1H-indazol-1-yl)-N-(1-(tert-butyldimethylsilyloxy)propan-2-yl)acetamido)acetate(358g) (140 mg, 40%) as an off-white solid; ¹H NMR (300 MHz, DMSO-d₆) δ9.39 (s, 1H), 8.38 and 8.36 (2s, 1H), 7.98-7.23 (m, 4H), 5.78-5.19 (m,2H), 4.48-3.55 (m, 7H), 1.49 (s, 9H), 1.27 (t, J=7.1 Hz) and 1.12 (t,J=7.1 Hz) (2t, 3H), 1.17 (d, J=6.7 Hz) and 1.04 (d, J=6.9 Hz) (2d, 3H),0.90 and 0.86 (2s, 9H), 0.11-0.00 (m, 6H); MS (ES+): 614.6 (M+Na).

Step-7: Preparation of(R)-2-(2-(5-(tert-butoxycarbonylamino)-3-carbamoyl-1H-indazol-1-yl)-N-(1-(tert-butyldimethylsilyloxy)propan-2-yl)acetamido)aceticacid (358h)

Reaction of (R)-ethyl2-(2-(5-(tert-butoxycarbonylamino)-3-carbamoyl-1H-indazol-1-yl)-N-(1-(tert-butyldimethylsilyloxy)propan-2-yl)acetamido)acetate(358g) (1.36 g, 2.298 mmol) with lithium hydroxide hydrate (0.59 g,13.79 mmol) according to the procedure reported in step-2 of Scheme 129gave after workup and purification(R)-2-(2-(5-(tert-butoxycarbonylamino)-3-carbamoyl-1H-indazol-1-yl)-N-(1-(tert-butyldimethylsilyloxy)propan-2-yl)acetamido)aceticacid (358h) (350 mg, 27%) as a brown solid; ¹H NMR (300 MHz, DMSO-d₆) δ9.38 (s, 1H), 8.37 (s, 1H), 7.69-7.23 (m, 4H), 5.76-5.12 (m, 2H),4.54-3.51 (m, 5H), 1.49 (s, 9H), 1.28-1.01 (m, 3H), 0.91 and 0.86 (2s,9H), 0.10-0.01 (m, 6H); MS (ES−): 562.7 (M−1).

Step-8: Preparation of tert-butyl1-(2-(((S)-1-(tert-butyldimethylsilyloxy)propan-2-yl)(2-((S)-1-(3-chloro-2-fluorophenyl)-3-(dimethylamino)propylamino)-2-oxoethyl)amino)-2-oxoethyl)-3-carbamoyl-1H-indazol-5-ylcarbamate(358i)

Reaction of(S)-2-(2-(5-(tert-butoxycarbonylamino)-3-carbamoyl-1H-indazol-1-yl)-N-(1-acid(358h) (20 mg, 0.035 mmol) with(S)-1-(3-chloro-2-fluorophenyl)-N3,N3-dimethylpropane-1,3-diamine (358f)(24.56 mg, 0.106 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup and purification by flash columnchromatography [silica gel eluting with dichloromethane/methanol (1:0 to9:1)] tert-butyl1-(2-(((S)-1-(tert-butyldimethylsilyloxy)propan-2-yl)(2-4S)-1-(3-chloro-2-fluorophenyl)-3-(dimethylamino)propylamino)-2-oxoethyl)amino)-2-oxoethyl)-3-carbamoyl-1H-indazol-5-ylcarbamate(358i) (10 mg, 36% for 4 steps) as a light yellow gum; MS (ES+): 776.7 &778.8 (M+Na).

Step-9: Preparation of5-amino-1-(2-((2-(((S)-1-(3-chloro-2-fluorophenyl)-3-(dimethylamino)propyl)amino)-2-oxoethyl)((R)-1-hydroxypropan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(358j)

Reaction of tert-butyl1-(2-(((S)-1-(tert-butyldimethylsilyloxy)propan-2-yl)(2-((S)-1-(3-chloro-2-fluorophenyl)-3-(dimethylamino)propylamino)-2-oxoethyl)amino)-2-oxoethyl)-3-carbamoyl-1H-indazol-5-ylcarbamate((358i)) (10 mg, 0.013 mmol) in Methanol (4 mL) with conc. HCl (0.032mL, 0.386 mmol) at RT for 15.5 h, gave after workup and purification byflash column chromatography [silica gel eluting with chloroform/CMA80(1:0 to 0:1)]5-amino-1-(2-((2-((S)-1-(3-chloro-2-fluorophenyl)-3-(dimethylamino)propylamino)-2-oxoethyl)((S)-1-hydroxypropan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(358j) (1.3 mg, 18%) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) (amixture of two rotamers) δ 8.91 (d, J=7.8 Hz) and 8.55 (d, J=8.0 Hz)(2d, 1H), 7.62-6.71 (m, 8H), 5.69-3.42 (m, 11H), 2.31-1.40 (m, 10H),1.10 (d, J=6.5 Hz) and 0.99 (d, J=6.9 Hz) (2d, 3H); ¹⁹F NMR (282 MHz,Methanol-d₄) δ −122.46, −122.63; MS (ES+): 562.6 (M+1) and 584.6 (M+Na);MS (ES−): 560.6 (M−1).

Preparation of1-(2-(((1H-imidazol-4-yl)methyl)(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-5-amino-1H-indazole-3-carboxamide(359f) Step-1: Preparation of methyl2-(((1-trityl-1H-imidazol-4-yl)methyl)amino)acetate (359b)

Compound 359b was prepared from 1-trityl-1H-imidazole-4-carbaldehyde(359a) (1 g, 2.84 mmol) and methyl 2-aminoacetate hydrochloride (0.360g, 2.84 mmol) According to the procedure reported in step-1 of Scheme24. This gave after workup and purification by flash columnchromatography [Silica gel, eluting with hexanes/ethyl acetate (1:0 to1:1), then dichloromethane/methanol (1:0 to 9:1)] methyl2-(41-trityl-1H-imidazol-4-yl)methyl)amino)acetate (359b) (84 mg, 7%) asa light brown gum, which was used as such for next step); MS (ES+):434.5 (M+Na)

Step-2: Preparation of methyl2-(2-(5-((tert-butoxycarbonyl)amino)-3-carbamoyl-1H-indazol-1-yl)-N-((1-trityl-1H-imidazol-4-yl)methyl)acetamido)acetate(359c)

Compound 359c was prepared from methyl2-(41-trityl-1H-imidazol-4-yl)methyl)amino)acetate (359b) (82 mg, 0.199mmol) and2-(5-((tert-butoxycarbonyl)amino)-3-carbamoyl-1H-indazol-1-yl)aceticacid (345c) (44.4 mg, 0.133 mmol) according to the procedure reported instep-3 of Scheme 2. This gave after workup and purification by flashcolumn chromatography [Silica gel, eluting with dichloromethane/methanol(1:0 to 19:1)] methyl2-(2-(5-((tert-butoxycarbonyl)amino)-3-carbamoyl-1H-indazol-1-yl)-N-((l-trityl-1H-imidazol-4-yl)methyl)acetamido)acetate(359c) (73 mg, 76%) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) (amixture of two rotamers) δ 9.39 (s, 1H), 8.38 (s, 1H), 7.61 (s, 1H),7.54-6.75 (m, 20H), 5.86 and 5.39 (2s, 2H), 4.64-3.96 (m, 4H), 3.66 and3.57 (2s, 3H), 1.50 and 1.49 (s, 9H); MS (ES+): 728.7 (M+1), 750.7,751.8 (M+Na).

Step-3: Preparation of2-(2-(5-((tert-butoxycarbonyl)amino)-3-carbamoyl-1H-indazol-1-yl)-N-((1-trityl-1H-imidazol-4-yl)methyl)acetamido)aceticacid (359d)

Compound 345d was prepared from methyl2-(2-(5-((tert-butoxycarbonyl)amino)-3-carbamoyl-1H-indazol-1-yl)-N-((1-trityl-1H-imidazol-4-yl)methyl)acetamido)acetate(359c) (69 mg, 0.095 mmol) and lithium hydroxide hydrate (24.36 mg,0.569 mmol) according to the procedure reported in step-2 of Scheme 129.This gave after workup 2-(2-(5-((tert-butoxycarbonyl)amino)-3-carbamoyl-1H-indazol-1-yl)-N-((1-trityl-1H-imidazol-4-yl)methyl)acetamido)aceticacid (359d) (55 mg, 81%) as a white solid; ¹H NMR (300 MHz, DMSO-d₆)(amixture of two rotamers) δ 12.70 (s, 1H), 9.39 (s, 1H), 8.38 (s, 1H),7.70-6.76 (m, 21H), 5.81 and 5.36 (2s, 2H), 4.61-3.88 (m, 4H), 1.495 and1.491 (2s, 9H); MS (ES+): 736.7 (M+Na).

Step-4: Preparation of (tert-butyl(3-carbamoyl-1-(2-((2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)((1-trityl-1H-imidazol-4-yl)methyl)amino)-2-oxoethyl)-1H-indazol-5-yl)carbamate(359e)

Compound 359e was prepared from2-(2-(5-((tert-butoxycarbonyl)amino)-3-carbamoyl-1H-indazol-1-yl)-N-((1-trityl-1H-imidazol-4-yl)methyl)acetamido)aceticacid (359d) (45 mg, 0.063 mmol) by reaction withN-(3-chloro-2-fluorobenzyl)-2-(cyclopropylamino)acetamide (10b) (32 mg,0.126 mmol) according to the procedure reported in step-3 of Scheme 2.This gave after workup and purification by flash column chromatography[Silica gel, eluting with dichloromethane/methanol (1:0 to 9:1)](tert-butyl(3-carbamoyl-1-(2-((2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)((1-trityl-1H-imidazol-4-yl)methyl)amino)-2-oxoethyl)-1H-indazol-5-yl)carbamate(359e) (38 mg, 63%), which used as such for next step; MS (ES+): 974.6 &976.6 (M+Na).

Step-5: Preparation of1-(2-(((1H-imidazol-4-yl)methyl)(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-5-amino-1H-indazole-3-carboxamide(359f)

Compound 359f was prepared from (tert-butyl(3-carbamoyl-1-(2-((2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)((1-trityl-1H-imidazol-4-yl)methyl)amino)-2-oxoethyl)-1H-indazol-5-yl)carbamate(359e) (38 mg, 0.040 mmol) by reaction with conc. HCl (0.1 mL) inmethanol (4 mL) according to the procedure reported in step-3 of Scheme292. This gave after workup and purification by flash columnchromatography [Silica gel, eluting with chloroform/CMA80 (1:0 to 0:1)]1-(2-(((1H-imidazol-4-yl)methyl)(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-5-amino-1H-indazole-3-carboxamide(359f) (8 mg, 32%) as a white solid. ¹H NMR (300 MHz, DMSO-d₆, a mixtureof two rotamers) δ 8.61 and 8.44 (2t, 1H), 7.82-7.74 (m, 1H), 7.54-7.40(m, 2H), 7.34-7.05 (m, 6H), 6.83-6.75 (m, 1H), 5.74 and 5.27 (2s, 2H),4.61 and 4.56 (2s, 2H), 4.42-4.26 (m, 4H), 4.04 and 3.94 (2s, 2H),2.97-2.67 (m, 1H), 0.93-0.57 (m, 4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ−121.52, −121.61; MS (ES+): 610.5 & 612.5 (M+1).

Preparation of5-amino-1-(2-((2-(((S)-1-(3-chloro-2-fluorophenyl)-3-hydroxypropyl)amino)-2-oxoethyl)((R)-1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide (360d) Step-1:Preparation of (S)-3-amino-3-(3-chloro-2-fluorophenyl)propan-1-ol (360a)

Reaction of (R)—N—((S)-1-(3-chloro-2-fluorophenyl)-3-hydroxypropyl)-2-methylpropane-2-sulfinamide (358c) (125 mg, 0.406 mmol) inMeOH (5 mL) with hydrogen chloride (0.203 mL, 0.812 mmol) (4 N in1,4-dioxane) at RT for 1 h, followed by evaporation of reaction mixtureunder reduced pressure gave(S)-3-amino-3-(3-chloro-2-fluorophenyl)propan-1-ol (360a), which wasused as such for next step; MS (ES+): 204.3 & 206.3 (M+1).

Step-2: Preparation of(S)-3-(tert-butyldimethylsilyloxy)-1-(3-chloro-2-fluorophenyl)propan-1-amine(360b)

Reaction of (S)-3-amino-3-(3-chloro-2-fluorophenyl)propan-1-01 (360a)(0.083 g, 0.406 mmol) in DMF (5 mL) with TBDMS-C₁ (0.092 g, 0.609 mmol)according to the procedure reported in step-1 of Scheme 328 gave afterworkup and purification(S)-3-(tert-butyldimethylsilyloxy)-1-(3-chloro-2-fluorophenyl)propan-1-amine(360b) (133 mg) as a yellow oil, which was used as such for next step;MS (ES+): 318.4 & 320.4 (M+Na).

Step-3: Preparation of tert-butyl1-((S)-11-((S)-1-(tert-butyldimethylsilyloxy)propan-2-yl)-7-(3-chloro-2-fluorophenyl)-2,2,3,3-tetramethyl-9,12-dioxo-4-oxa-8,11-diaza-3-silatridecan-13-yl)-3-carbamoyl-1H-indazol-5-ylcarbamate(360c)

Reaction of(S)-2-(2-(5-(tert-butoxycarbonylamino)-3-carbamoyl-1H-indazol-1-yl)-N-(1-(tert-butyldimethylsilyloxy)propan-2-yl)acetamido)aceticacid (358h) (20 mg, 0.035 mmol) with(S)-3-(tert-butyldimethylsilyloxy)-1-(3-chloro-2-fluorophenyl)propan-1-amine(360b) (33.8 mg, 0.106 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica gel eluting with dichloromethane/methanol (1:0 to19:1)] tert-butyl1-((S)-11-((S)-1-(tert-butyldimethylsilyloxy)propan-2-yl)-7-(3-chloro-2-fluorophenyl)-2,2,3,3-tetramethyl-9,12-dioxo-4-oxa-8,11-diaza-3-silatridecan-13-yl)-3-carbamoyl-1H-indazol-5-ylcarbamate(360c) (29 mg) as a colorless gum; MS (ES+): 885.7 (M+Na).

Step-4: Preparation of5-amino-1-(2-((2-((S)-1-(3-chloro-2-fluorophenyl)-3-hydroxypropylamino)-2-oxoethyl)((S)-1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(360d)

Reaction of tert-butyl1-((S)-11-((S)-1-(tert-butyldimethylsilyloxy)propan-2-yl)-7-(3-chloro-2-fluorophenyl)-2,2,3,3-tetramethyl-9,12-dioxo-4-oxa-8,11-diaza-3-silatridecan-13-yl)-3-carbamoyl-1H-indazol-5-ylcarbamate(360c) (29 mg, 0.034 mmol) in methanol (4 mL) with conc. HCl (0.028 mL,0.336 mmol) at RT for 19 h gave after workup and purification by flashcolumn chromatography [silica gel eluting with chloroform/CMA80 (1:0 to0:1)]5-amino-1-(2-((2-((S)-1-(3-chloro-2-fluorophenyl)-3-hydroxypropylamino)-2-oxoethyl)((S)-1-hydroxypropan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamideas a white solid (360d) (3 mg, 6% for 4 steps); ¹H NMR (300 MHz,DMSO-d₆) (a mixture of two rotamers) δ 8.86 (d) and 8.50 (d, J=7.6 Hz)(2d, 1H), 7.56-6.71 (m, 8H), 5.60-3.20 (m, 14H), 2.03-1.65 (m, 2H), 1.10(d, J=6.3 Hz) and 0.98 (d, J=6.8 Hz) (2d, 3H); ¹⁹F NMR (282 MHz,DMSO-d₆) δ −121.68, −121.87; MS (ES+): 557.2 (M+Na); MS (ES−): 533.6(M−1).

Preparation of5-amino-1-(2-((2-(((R)-1-(3-chloro-2-fluorophenyl)-3-(dimethylamino)propyl)amino)-2-oxoethyl)((R)-1-hydroxypropan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(361h) Step-1: Preparation of (S)-tert-butyl3-(3-chloro-2-fluorophenyl)-3-((R)-1,1-dimethylethyl-sulfinamido)propanoate(361b)

Reaction of(S,E)-N-(3-chloro-2-fluorobenzylidene)-2-methylpropane-2-sulfinamide(361a) (500 mg, 1.91 mmol; prepared according to the procedure reportedby Lain, Patrick Y. S. et al; in PCT 1111. Appl, 2013022814, 14 Feb.2013) with (2-tert-butoxy-2-oxoethyl)zinc(II) chloride (9.93 mL, 4.97mmol) according to the procedure reported in step-1 of Scheme 358 gaveafter workup and purification (R)-tert-butyl3-(3-chloro-2-fluorophenyl)-3-((S)-1,1-dimethylethyl-sulfinamido)propanoateas a colorless gum (361b) (675 mg) as a colorless oil which was used assuch for next step. MS (ES−): 412.4 & 414.5 (M+Cl).

Step-2: Preparation of(R)-3-(3-chloro-2-fluorophenyl)-3-((S)-1,1-dimethylethyl-sulfinamido)propylmethanesulfonate (361c)

Reaction of(S)—N—((R)-1-(3-chloro-2-fluorophenyl)-3-hydroxypropyl)-2-methylpropane-2-sulfinamide(360 mg, 1.17 mmol) (crude) with methanesulfonyl chloride (0.100 mL,1.287 mmol) according to the procedure reported in step-2 of Scheme 358gave after workup and purification(R)-3-(3-chloro-2-fluorophenyl)-3-((S)-1,1-dimethylethyl-sulfinamido)propylmethanesulfonate as a colorless gum (361c) (421 mg, used as such fornext step). MS (ES⁺): 386.4 & 388.4 (M+1).

Step-3: Preparation of(R)-3-(3-chloro-2-fluorophenyl)-3-((S)-1,1-dimethylethyl-sulfinamido)propylmethanesulfonate (361d)

Reaction of(S)—N—((R)-1-(3-chloro-2-fluorophenyl)-3-hydroxypropyl)-2-methylpropane-2-sulfinamide(360 mg, 1.17 mmol, crude) with methanesulfonyl chloride (0.10 mL, 1.287mmol) according to the procedure reported in step-3 of Scheme 358 gaveafter workup and purification(R)-3-(3-chloro-2-fluorophenyl)-3-((S)-1,1-dimethylethyl-sulfinamido)propylmethanesulfonate (361d) (421 mg) as a colorless gum, which was used assuch for next step; MS (ES+): 386.4 & 388.4 (M+1).

Step-4: Preparation of(S)—N—((R)-1-(3-chloro-2-fluorophenyl)-3-(dimethylamino)propyl)-2-methylpropane-2-sulfinamide(361e)

Reaction of(R)-3-(3-chloro-2-fluorophenyl)-3-((S)-1,1-dimethylethylsulfinamido)propylmethanesulfonate (120 mg, 0.311 mmol) (361d) with dimethylamine (2M inTHF, 3.42 mL, 6.84 mmol) according to the procedure reported in step-4of Scheme 358 gave after workup and purification(S)—N—((R)-1-(3-chloro-2-fluorophenyl)-3-(dimethylamino)propyl)-2-methylpropane-2-sulfinamide(361e) (131 mg) as a yellow gum which was used as such for next stepwithout further purification); MS (ES+): 335.4 & 337.4 (M+1).

Step-5: Preparation of(R)-1-(3-chloro-2-fluorophenyl)-N3,N3-dimethylpropane-1,3-diamine (361f)

Reaction of(S)—N—((R)-1-(3-chloro-2-fluorophenyl)-3-(dimethylamino)propyl)-2-methylpropane-2-sulfinamide(361e) (0.104 g, 0.311 mmol) with hydrogen chloride (0.156 mL, 0.622mmol, 4 N in 1,4-dioxane) according to the procedure reported in step-5of Scheme 358 gave after workup and purification(R)-1-(3-chloro-2-fluorophenyl)-N3,N3-dimethylpropane-1,3-diamine(361e), which was used as such for next step; MS (ES+): 231.4 & 333.3(M+1).

Step-6: Preparation of tert-butyl1-(2-(((R)-1-(tert-butyldimethylsilyloxy)propan-2-yl)(2-((R)-1-(3-chloro-2-fluorophenyl)-3-(dimethylamino)propylamino)-2-oxoethyl)amino)-2-oxoethyl)-3-carbamoyl-1H-indazol-5-ylcarbamate(361g)

Reaction of(R)-2-(2-(5-(tert-butoxycarbonylamino)-3-carbamoyl-1H-indazol-1-yl)-N-(1-(tert-butyldimethylsilyloxy)propan-2-yl)acetamido)aceticacid (358h) (58.4 mg, 0.104 mmol) with(R)-1-(3-chloro-2-fluorophenyl)-N3,N3-dimethylpropane-1,3-diamine (361f)(71.8 mg, 0.311 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup and purification by flash columnchromatography [silica gel with dichloromethane/methanol (1:0 to 9:1)]tert-butyl1-(2-(((R)-1-(tert-butyldimethylsilyloxy)propan-2-yl)(2-((R)-1-(3-chloro-2-fluorophenyl)-3-(dimethylamino)propylamino)-2-oxoethyl)amino)-2-oxoethyl)-3-carbamoyl-1H-indazol-5-ylcarbamate(361g) (11 mg, 14% for 6 steps) as a white solid; MS (ES+): 776.6 &778.6 (M+1).

Step-7: Preparation of5-amino-1-(2-((2-(((R)-1-(3-chloro-2-fluorophenyl)-3-(dimethylamino)propyl)amino)-2-oxoethyl)((R)-1-hydroxypropan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(361h)

Reaction of tert-butyl1-(2-(((S)-1-(tert-butyldimethylsilyloxy)propan-2-yl)(2-((R)-1-(3-chloro-2-fluorophenyl)-3-(dimethylamino)propylamino)-2-oxoethyl)amino)-2-oxoethyl)-3-carbamoyl-1H-indazol-5-ylcarbamate(361g) (11 mg, 0.014 mmol) with conc. HCl (0.071 mL, 0.850 mmol)according to the procedure reported in step-9 of Scheme 358 gave afterworkup and purification by flash column chromatography [silica gel withchloroform/CMA80 (1:0 to 0:1)]5-amino-1-(2-((2-((R)-1-(3-chloro-2-fluorophenyl)-3-(dimethylamino)propylamino)-2-oxoethyl)((R)-1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(361h) (5 mg, 63%) as a white solid; ¹H NMR (300 MHz, DMSO-d₆) (amixture of two rotamers) δ 8.99 and 8.59 (2d, J=8.1 Hz, 1H), 7.61-6.67(m, 8H), 5.61-3.40 (m, 11H), 2.48-1.76 (m, 10H), 1.11 (d, J=6.5 Hz) and0.85 (d, J=6.9 Hz) (2d, 3H); MS (ES+): 562.6 & 564.7 (M+1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3,6-dicarboxamide(362a)

To a solution of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-6-cyano-1H-indazole-3-carboxamide(356c) (37 mg, 0.077 mmol) in Ethanol (4 mL) was added conc. NH₄OH (1.5mL), hydrogen peroxide (0.027 mL, 0.306 mmol) and stirred at RT for 15h. The reaction mixture was concentrated to dryness. The crude productwas purified by flash column chromatography [silica gel, eluting withdichloromethane/methanol (1:0 to 9:1)] to give1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3,6-dicarboxamide(362a) (34 mg, 89%); ¹H NMR (300 MHz, DMSO-d₆) δ 8.55 (t, J=5.8 Hz, 1H),8.28-8.13 (m, 2H), 8.06 (s, 1H), 7.85-7.71 (m, 2H), 7.53 (s, 1H),7.49-7.38 (m, 2H), 7.26-7.19 (m, 1H), 7.13-7.06 (m, 1H), 5.72 (s, 2H),4.32 (d, J=5.7 Hz, 2H), 4.00 (s, 2H), 3.14-2.99 (m, 1H), 1.08-0.85 (m,4H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.55; MS (ES+): 523.4 & 525.4(M+Na).

Preparation of5-amino-1-(2-((2-(((R)-1-(3-chloro-2-fluorophenyl)-3-hydroxypropyl)amino)-2-oxoethyl)((R)-1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(363d) Step-1: Preparation of(R)-3-amino-3-(3-chloro-2-fluorophenyl)propan-1-ol (363a)

Reaction of(S)—N—((R)-1-(3-chloro-2-fluorophenyl)-3-hydroxypropyl)-2-methylpropane-2-sulfinamide(361c) (150 mg, 0.487 mmol) with hydrogen chloride (0.244 mL, 0.975mmol) (4 N in 1,4-dioxane) according to the procedure reported in step-1of Scheme 360 gave after workup(R)-3-amino-3-(3-chloro-2-fluorophenyl)propan-1-ol (363a), which wasused as such for next step without further purification; MS (ES+): 204.3(M+1).

Step-2: Preparation of(R)-3-(tert-butyldimethylsilyloxy)-1-(3-chloro-2-fluorophenyl)propan-1-amine(363b)

Reaction of (R)-3-amino-3-(3-chloro-2-fluorophenyl)propan-1-ol (363a)(0.099 g, 0.487 mmol) in DMF (6 mL) with TBDMS-Cl (0.11 g, 0.731 mmol)according to the procedure reported in step-2 of Scheme 360 gave afterworkup(R)-3-(tert-butyldimethylsilyloxy)-1-(3-chloro-2-fluorophenyl)propan-1-amineas a yellow oil (363b) (139 mg), which was used as such for next step.

Step-3: Preparation of tert-butyl1-((R)-11-((R)-1-(tert-butyldimethylsilyloxy)propan-2-yl)-7-(3-chloro-2-fluorophenyl)-2,2,3,3-tetramethyl-9,12-dioxo-4-oxa-8,11-diaza-3-silatridecan-13-yl)-3-carbamoyl-1H-indazol-5-ylcarbamate(363c)

Reaction of(R)-2-(2-(5-(tert-butoxycarbonylamino)-3-carbamoyl-1H-indazol-1-yl)-N-(1-(tert-butyldimethylsilyloxy)propan-2-yl)acetamido)aceticacid (358h) (80 mg, 0.142 mmol) with(R)-3-(tert-butyldimethylsilyloxy)-1-(3-chloro-2-fluorophenyl)propan-1-amine(363b) (135 mg, 0.425 mmol) (crude) according to the procedure reportedin step-3 of Scheme 360 gave after workup and purification by flashcolumn chromatography [silica gel, eluting with dichloromethane/methanol(1:0 to 19:1)] tert-butyl1-((R)-11-((R)-1-(tert-butyldimethylsilyloxy)propan-2-yl)-7-(3-chloro-2-fluorophenyl)-2,2,3,3-tetramethyl-9,12-dioxo-4-oxa-8,11-diaza-3-silatridecan-13-yl)-3-carbamoyl-1H-indazol-5-ylcarbamate(363c) (85 mg) as an off-white solid; MS (ES+): 885.8 & 887.9 (M+Na).

Step-4: Preparation of5-amino-1-(2-((2-((R)-1-(3-chloro-2-fluorophenyl)-3-hydroxypropylamino)-2-oxoethyl)((R)-1-hydroxypropan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(363d)

Reaction of tert-butyl1-((R)-11-((R)-1-(tert-butyldimethylsilyloxy)propan-2-yl)-7-(3-chloro-2-fluorophenyl)-2,2,3,3-tetramethyl-9,12-dioxo-4-oxa-8,11-diaza-3-silatridecan-13-yl)-3-carbamoyl-1H-indazol-5-ylcarbamate(363c) (71 mg, 0.082 mmol) with conc. HCl (0.206 mL, 2.466 mmol)according to the procedure reported in step-4 of Scheme 360 gave afterworkup and purification by flash column chromatography [silica gel,eluting with chloroform/CMA80 (1:0 to 0:1)]5-amino-1-(2-((2-((R)-1-(3-chloro-2-fluorophenyl)-3-hydroxypropylamino)-2-oxoethyl)((R)-1-hydroxypropan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamideas a light brown solid (363d) (13 mg, 21% for 4 steps); ¹H NMR (300 MHz,DMSO-d₆) (mixture of two rotamers) δ 8.89 (d, J=7.7 Hz) and 8.52 (d,J=7.7 Hz) (2d, 1H), 7.62-6.68 (m, 8H), 5.66-3.10 (m, 14H), 2.03-1.68 (m,2H), 1.08 (d, J=6.4 Hz) and 0.83 (d, J=6.9 Hz) (2d, 3H); ¹⁹F NMR (282MHz, DMSO-d₆) δ −121.75, −122.15; MS (ES+): 557.4 & 559.6 (M+Na); MS(ES−): 533.5 & 535.6 (M+Cl).

Preparation of1-(2-(((1H-imidazol-4-yl)methyl)(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-5-amino-1H-indazole-3-carboxamide(364b) Step-1: Preparation of tert-butyl(3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((1-trityl-1H-imidazol-4-yl)methyl)amino)-2-oxoethyl)-1H-indazol-5-yl)carbamate(364a)

Compound 364a was prepared from2-(2-(5-((tert-butoxycarbonyl)amino)-3-carbamoyl-1H-indazol-1-yl)-N-((1-trityl-1H-imidazol-4-yl)methyl)acetamido)aceticacid (359d) (40 mg, 0.056 mmol) by reaction with(3-chloro-2-fluorophenyl)methanamine (9d) (0.018 mL, 0.140 mmol)according to the procedure reported in step-3 of Scheme 2. This gaveafter workup and purification by flash column chromatography [Silicagel, eluting with dichloromethane/methanol (1:0 to 19:1)] tert-butyl(3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((1-trityl-1H-imidazol-4-yl)methyl)amino)-2-oxoethyl)-1H-indazol-5-yl)carbamate(364a) (60 mg) as an off-white solid; MS (ES+): 877.7 (M+Na).

Step-2: Preparation of1-(2-(((1H-imidazol-4-yl)methyl)(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-5-amino-1H-indazole-3-carboxamide(364b)

Compound 364b was prepared from tert-butyl(3-carbamoyl-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((1-trityl-1H-imidazol-4-yl)methyl)amino)-2-oxoethyl)-1H-indazol-5-yl)carbamate(364a) (55 mg, 0.064 mmol) by reaction with conc. HCl (0.214 mL, 2.57mmol) in methanol (5 mL) according to the procedure reported in step-3of Scheme 292. This gave after workup and purification by flash columnchromatography [Silica gel, eluting with chloroform/CMA80 (1:0 to 1:2)]to give1-(2-(((1H-imidazol-4-yl)methyl)(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxo ethyl)-5-amino-1H-indazole-3-carboxamide (364b) (15mg, 57% for two steps) as a light brown solid; ¹H NMR (300 MHz, DMSO-d₆,mixture of two rotamers) δ 12.11 & 11.97 (2s, 1H), 8.91 & 8.66 (2t,J=6.0 Hz, 1H), 7.87-6.71 (m, 10H), 5.80-4.94 (m, 4H), 4.71-3.82 (m, 6H);¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.41, −121.64; MS (ES+): 513.4 (M+1); MS(ES−): 511.5 (M−1).

Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((l-methylpiperidin-4-yl)methyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(365b) Step 1: Preparation ofN-(3-chloro-2-fluorobenzyl)-2-(((1-methylpiperidin-4-yl)methyl)amino)acetamide(365a)

Reaction of 2-chloro-N-(3-chloro-2-fluorobenzyl)acetamide (35b) (604 mg,2.56 mmol) with (1-methylpiperidin-4-yl)methanamine (820 mg, 6.4 mmol)according to the procedure reported in step-2 of Scheme 35 gave afterworkup and purification by flash column chromatography [Silica gel, 12 geluting with methanol in DCM from 0-30%)N-(3-chloro-2-fluorobenzyl)-2-(((1-methylpiperidin-4-yl)methyl)amino)acetamide(365a) (535 mg, 64% yield) as a clear oil. ¹H NMR (300 MHz, DMSO-d₆) δ8.30 (t, J=6.1 Hz, 1H, D₂O exchangeable), 7.47 (td, J=7.6, 1.8 Hz, 1H),7.32-7.23 (m, 1H), 7.23-7.09 (m, 1H), 4.36 (d, J=6.0 Hz, 2H), 3.21-3.04(m, 3H), 2.77-2.60 (m, 2H), 2.31 (d, J=6.5 Hz, 2H), 2.10 (s, 4H), 1.75(td, J=11.5, 2.5 Hz, 2H), 1.68-1.55 (m, 2H), 1.18-0.94 (m, 2H); MS(ES+): 328.3 (M+1); (ES−): 326.4 (M−1).

Step 2: Preparation of1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((1-methylpiperidin-4-yl)methyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(365b)

Reaction ofN-(3-chloro-2-fluorobenzyl)-2-(((1-methylpiperidin-4-yl)methyl)amino)acetamide(365a) (150 mg, 0.46 mmol) with 2-(3-carbamoyl-1H-indazol-1-yl)aceticacid (2e) (120 mg, 0.55 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [Silica gel, 12 g eluting with CMA80 in CHCl₃ from 0 to60%]1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)((1-methylpiperidin-4-yl)methyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(365b) (65 mg, 27% yield) as a white solid, ¹H NMR (300 MHz, DMSO-d₆) δ10.24 (s, 1H, D₂O exchangeable), 9.04 (t, J=5.8 Hz, 1H, D₂Oexchangeable), 8.18 (d, J=8.1 Hz, 1H), 7.71 (s, 1H), 7.62-7.34 (m, 5H),7.30-7.06 (m, 2H), 5.62-5.38 (m, 2H), 4.71 (s, 2H), 4.53-4.23 (m, 4H),3.41 (dd, J=30.9, 10.2 Hz, 2H), 3.17 (d, J=6.7 Hz, 1H), 2.81-2.63 (m,4H), 2.05-1.88 (m, 1H), 1.80-1.63 (m, 2H), 1.48-1.28 (m, 1H); MS (ES+):529.3 (M+1); (ES−): 563.3 (M+Cl).

Preparation of5-amino-1-(2-((2-(((S)-1-(3-chloro-2-fluorophenyl)-2-(dimethylamino)ethyl)amino)-2-oxoethyl)((R)-1-hydroxypropan-2-yl)-amino)-2-oxoethyl)-1H-indazole-3-carboxamide(366f) Step-1: Preparation of (S)-tert-butyl1-(3-chloro-2-fluorophenyl)-2-hydroxyethylcarbamate (366a)

To a solution of (S)-2-amino-2-(3-chloro-2-fluorophenyl)ethanolhydrochloride (328a) (800 mg, 3.54 mmol) in DCM (30 mL) and MeOH (15 mL)was added di-tert-butyl dicarbonate (946 mg, 4.25 mmol), triethylamine(0.986 mL, 7.08 mmol) and stirred at RT for 20 h. The reaction mixturewas diluted with dichloromethane (100 mL), washed with water (50 mL),dried, filtered, concentrated in vacuum to give (5)-tert-butyl1-(3-chloro-2-fluorophenyl)-2-hydroxyethylcarbamate (366a) (1.083 g) asa white solid which was used as such for next step. MS (ES+): 312.3 &314.2 (M+Na).

Step-2: Preparation of(S)-2-(tert-butoxycarbonylamino)-2-(3-chloro-2-fluorophenyl)ethylmethanesulfonate (366b)

Reaction of (5)-tert-butyl1-(3-chloro-2-fluorophenyl)-2-hydroxyethylcarbamate (366a) (1.026 g,3.54 mmol) with methanesulfonyl chloride (0.303 mL, 3.89 mmol) accordingto the procedure reported in step-3 of Scheme 358 gave after workup(S)-2-(tert-butoxycarbonylamino)-2-(3-chloro-2-fluorophenyl)ethylmethanesulfonate (366b) (1.317 g) as a white solid which was used assuch for next step. ¹H NMR (300 MHz, DMSO-d₆) δ 7.87 (d, J=8.7 Hz, 1H),7.56 (t, J=7.9 Hz, 1H), 7.44 (t, J=7.1 Hz, 1H), 7.27 (t, J=7.9 Hz, 1H),5.25-5.09 (m, 1H), 4.35-4.19 (m, 2H), 3.19 (s, 3H), 1.37 (s, 9H); ¹⁹FNMR (282 MHz, DMSO-d₆) δ −121.15; MS (ES+): 390.2 & 392.2 (M+Na).

Step-3: Preparation of (5)-tert-butyl1-(3-chloro-2-fluorophenyl)-2-(dimethyl-amino)ethylcarbamate (366c)

Reaction of(S)-2-(tert-butoxycarbonylamino)-2-(3-chloro-2-fluorophenyl)ethylmethanesulfonate (366b) (120 mg, 0.326 mmol) with dimethylamine (2M inTHF, 3.59 mL, 7.18 mmol) according to the procedure reported in step-4of Scheme 358 gave after workup and purification by flash columnchromatography [silica gel, eluting with hexanes/ethyl acetate (1:0 to1:1)] (5)-tert-butyl1-(3-chloro-2-fluorophenyl)-2-(dimethyl-amino)ethylcarbamate as a browngum (366c) (27 mg, 28% for 3 steps). MS (ES+): 317.3 (M+1). Another sideproduct (S)-4-(3-chloro-2-fluorophenyl)oxazolidin-2-one was also formedfrom this reaction, MS (ES⁻): 214.2 & 216.1 (M−1).

Step-4: Preparation of(S)-1-(3-chloro-2-fluorophenyl)-N2,N2-dimethylethane-1,2-diamine (366d)

Reaction of (5)-tert-butyl1-(3-chloro-2-fluorophenyl)-2-(dimethylamino)ethylcarbamate (366c) (22mg, 0.069 mmol) with 2,2,2-trifluoroacetic acid (0.375 mL, 4.86 mmol)according to the procedure reported in step-2 of Scheme 2 gave afterworkup (S)-1-(3-chloro-2-fluorophenyl)-N2,N2-dimethylethane-1,2-diamine(366d), which used as such for next step.

Step-5: Preparation of tert-butyl1-(2-(((R)-1-(tert-butyldimethylsilyloxy)propan-2-yl)(2-((S)-1-(3-chloro-2-fluorophenyl)-2-(dimethylamino)ethylamino)-2-oxoethyl)amino)-2-oxoethyl)-3-carbamoyl-1H-indazol-5-ylcarbamate(366e)

Reaction of(R)-2-(2-(5-(tert-butoxycarbonylamino)-3-carbamoyl-1H-indazol-1-yl)-N-(1-(tert-butyldimethylsilyloxy)propan-2-yl)acetamido)aceticacid (358h) (0.051 g, 0.090 mmol) with(S)-1-(3-chloro-2-fluorophenyl)-N2,N2-dimethylethane-1,2-diamine (366d)(0.015 g, 0.069 mmol) according to the procedure reported in step-3 ofScheme 2 gave after workup and purification by flash columnchromatography [silica gel, eluting with chloroform/CMA80 (1:0 to 1:1)]tert-butyl1-(2-(((R)-1-(tert-butyldimethylsilyloxy)propan-2-yl)(2-((S)-1-(3-chloro-2-fluorophenyl)-2-(dimethylamino)ethylamino)-2-oxoethyl)amino)-2-oxoethyl)-3-carbamoyl-1H-indazol-5-ylcarbamate(366e) (17 mg) as a yellow solid; MS (ES+): 762.5 & 764.4 (M+1).

Step-6: Preparation of5-amino-1-(2-((2-((S)-1-(3-chloro-2-fluorophenyl)-2-(dimethylamino)ethylamino)-2-oxoethyl)((R)-1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(366f)

Reaction of tert-butyl1-(2-(((R)-1-(tert-butyldimethylsilyloxy)propan-2-yl)(2-((S)-1-(3-chloro-2-fluorophenyl)-2-(dimethylamino)ethylamino)-2-oxoethyl)amino)-2-oxoethyl)-3-carbamoyl-1H-indazol-5-ylcarbamate(366f) (17 mg, 0.022 mmol) with conc. HCl (0.111 mL, 1.338 mmol)according to the procedure reported in step-4 of Scheme 360 gave afterworkup and purification by flash column chromatography [silica gel,eluting with chloroform/CMA80 (1:0 to 0:1)]5-amino-1-(2-((2-((S)-1-(3-chloro-2-fluorophenyl)-2-(dimethylamino)ethylamino(366g) (8 mg, 21% for 3 steps) as a light pink solid; ¹H NMR (300 MHz,DMSO-d₆, a mixture of two rotamers) δ 7.71-6.74 (m, 8H), 5.63-3.40 (m,11H), 2.80-2.00 (m, 8H), 1.10 (d, J=6.4 Hz) and 0.86 (d, J=6.8 Hz) (2d,3H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −120.003, −120.009; MS (ES+): 548.4(M+1) & 570.5 (M+Na).

Preparation of5-amino-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)ethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(367g) Step-1: Preparation of tert-butyl2-((3-chloro-2-fluorobenzyl)amino)acetate (367a)

Compound 367a was prepared from (3-chloro-2-fluorophenyl)methanamine(9d) (4.06 g, 25.4 mmol) using K₂CO₃ (5.68 g, 40.7 mmol) and tert-butyl2-chloroacetate (3 mL, 20.35 mmol) according to the procedure reportedin step-1 of Scheme 43. This gave after workup and purification by flashcolumn chromatography [silica gel, eluting with hexanes/ethyl acetate(1:0 to 4:1)] tert-butyl 2-((3-chloro-2-fluorobenzyl)amino)acetate(367a) (2.78 g, 50%) as a colorless oil; ¹H NMR (300 MHz, DMSO-d₆) δ7.51-7.34 (m, 2H), 7.19 (td, J=7.8, 1.1 Hz, 1H), 3.78 (s, 2H), 3.20 (s,2H), 1.40 (s, 9H); MS (ES+): 274.3 & 276.2 (M+1).

Step-2: Preparation of 2-((3-chloro-2-fluorobenzyl)amino)ethanol (367b)

Compound 367b was prepared from tert-butyl2-((3-chloro-2-fluorobenzyl)amino)acetate (367a) (1.608 g, 5.87 mmol)and lithium borohydride (8.81 mL, 17.62 mmol, 2M in THF) according tothe procedure reported in step-2 of Scheme 358. This gave after workup2-((3-chloro-2-fluorobenzyl)amino)ethanol (367b) (1.175 g) as acolorless gum which was used as such for next step; MS (ES+): 204.2 &206.2 (M+1).

Step-3: Preparation of tert-butyl3-chloro-2-fluorobenzyl(2-hydroxyethyl)carbamate (367c)

To a solution of 2-(3-chloro-2-fluorobenzylamino)ethanol (367b) (1.1 g,5.40 mmol) in DCM (40 mL) and MeOH (20 mL) was added di-tert-butyldicarbonate (1.444 g, 6.48 mmol) triethylamine (1.506 mL, 10.80 mmol)and stirred at RT for 20 h. The reaction mixture was diluted withdichloromethane (120 mL), washed with water (60 mL), dried, filtered,concentrated in vacuum and purified by flash column chromatography[silica gel, eluting with dichloromethane/methanol (1:0 to 19:1)] togive tert-butyl 3-chloro-2-fluorobenzyl(2-hydroxyethyl)carbamate (367c)(713 mg) as a colorless oil which was used as such for next step; MS(ES+): 326.3 (M+Na).

Step-4: Preparation of2-((tert-butoxycarbonyl)(3-chloro-2-fluorobenzyl)amino)ethylmethanesulfonate (367d)

Compound 367d was prepared from tert-butyl3-chloro-2-fluorobenzyl(2-hydroxyethyl)carbamate (367c) (162 mg, 0.526mmol) triethylamine (0.147 mL, 1.053 mmol) and methanesulfonyl chloride(0.045 mL, 0.579 mmol) according to the procedure reported in step-3 ofScheme 358. This gave after workup2-((tert-butoxycarbonyl)(3-chloro-2-fluorobenzyl)amino)ethylmethanesulfonate (367d) (484 mg) as a colorless gum which was used assuch for next step.

Step-5: Preparation of tert-butyl3-chloro-2-fluorobenzyl(2-(cyclopropylamino)ethyl)carbamate (367e)

A solution of2-((tert-butoxycarbonyl)(3-chloro-2-fluorobenzyl)amino)ethylmethanesulfonate (367d)

(270 mg, 0.707 mmol) in DMF (10 mL) was added cyclopropanamine (1.084mL, 15.56 mmol) and heated with stirring at 80° C. in a sealed tube for2 h. The reaction mixture was cooled to RT, diluted with ethyl acetate(100 mL), washed with water (2×50 mL), brine (50 mL), dried, filtered,concentrated in vacuum and purified by flash column chromatography[silica gel, eluting with hexanes/ethyl acetate (1:0 to 1:1)] to givetert-butyl 3-chloro-2-fluorobenzyl(2-(cyclopropylamino)ethyl)-carbamate(367e) contaminated with 3-(3-chloro-2-fluorobenzyl)oxazolidin-2-one (90mg, molar ratio: 1:5 based on ¹H NMR, 23% by weight of the desiredproduct, 3.8% yield for 4 steps) as a colorless oil which was used assuch for next step. MS (ES+): 343.3 & 345.3 (M+1).

Step-6: Preparation of tert-butyl(2-(2-(5-((tert-butoxycarbonyl)amino)-3-carbamoyl-1H-indazol-1-yl)-N-cyclopropylacetamido)ethyl)(3-chloro-2-fluorobenzyl)carbamate(367f)

Reaction of2-(5-((tert-butoxycarbonyl)amino)-3-carbamoyl-1H-indazol-1-yl)aceticacid (345c) (35 mg, 0.11 mmol) with tert-butyl3-chloro-2-fluorobenzyl(2-(cyclopropylamino)ethyl)carbamate (367e) (19mg, 0.05 mmol) according to the procedure reported in step-3 of Scheme 2gave after workup and purification by flash column chromatography[silica gel with dichloromethane/methanol (1:0 to 19:1)] tert-butyl(2-(2-(5-((tert-butoxycarbonyl)amino)-3-carbamoyl-1H-indazol-1-yl)-N-cyclopropylacetamido)ethyl)(3-chloro-2-fluorobenzyl)carbamate(367f) (24 mg, 66%) as a colorless gum; MS (ES+): 681.3 & 683.4 (M+Na).

Step-7: Preparation of5-amino-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)ethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(367g)

Compound 367g was prepared from tert-butyl(2-(2-(5-((tert-butoxycarbonyl)amino)-3-carbamoyl-1H-indazol-1-yl)-N-cyclopropylacetamido)ethyl)(3-chloro-2-fluorobenzyl)carbamate(367f) (24 mg, 0.036 mmol) by reaction with conc. HCl (0.152 mL, 1.82mmol) in methanol (4 mL) according to the procedure reported in step-3of Scheme 292. This gave after workup and purification by flash columnchromatography [Silica gel, eluting with chloroform/CMA80 (1:0 to 1:1)5-amino-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)ethyl)(cyclopropyl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(367g) (9 mg, 54%) as a brown solid; ¹H NMR (300 MHz, DMSO-d₆) δ7.65-7.19 (m, 6H), 7.12 (s, 1H), 6.80 (dd, J=8.8, 2.1 Hz, 1H), 5.52 (s,2H), 4.07 (s, 2H), 3.66-3.53 (m, 2H), 3.12-3.03 (m, 1H), 3.03-2.87 (m,2H), 1.06-0.89 (m, 4H); ¹⁹F NMR (282 MHz, Methanol-d₄) δ −120.77; MS(ES+): 481.0 (M+Na).

Preparation of(R)-5-amino-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(368a)

To a solution of (R)-tert-butyl(1-(2-((1-((tert-butyldimethylsilyl)oxy)propan-2-yl)(2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)amino)-2-oxoethyl)-3-carbamoyl-1H-indazol-5-yl)carbamate(345d)

(220 mg, 0.312 mmol) in MeOH (25 mL) was added hydrogen chloride (1.040mL, 12.48 mmol) and stirring at RT for 15 h. The reaction mixture wasconcentrated to dryness and purified by flash column chromatography[silica gel, eluting with chloroform/DMA80 (1:0 to 1:1)] followed byreverse-phase combiflash column chromatography with water (0.1%HCl)/acetonitrile (1:0 to 1:1) to give(R)-5-amino-1-(2-((2-((3-chloro-2-fluorobenzyl)amino)-2-oxoethyl)(1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(368a) (61 mg, 37%) as an off-white solid; ¹H NMR (300 MHz, DMSO-d₆ (amixture of two rotamers) δ 8.92 (t, J=5.6 Hz) and 8.60 (t, J=5.7 Hz((2t, 1H), 8.14 (s, 1H), 7.75 (s, 1H), 7.67-6.92 (m, 6H), 5.74-5.37 (m,2H), 4.58-3.68 (m, 5H), 3.60-3.10 (m, 2H), 1.16 (d, J=6.4 Hz) and 0.96(d, J=6.9 Hz) (2d, 3H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.23, −121.64;MS (ES+): 513.3 & 515.3 (M+Na); MS (ES⁻): 525.2 & 527.3 (M+Cl); AnalysisCalculated for C₂₂H24ClFN₆O₄.1.0 HCl.2.5H2O: C, 46.16; H, 5.28; N,14.68; Cl, 12.39; Found: C, 45.98; H, 5.00; N, 14.50; Cl, 12.44.

Preparation of5-amino-1-(2-((2-((R)-1-(3-chloro-2-fluorophenyl)-2-hydroxyethylamino)-2-oxoethyl)((R)-1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(369f) Step-1: Preparation of(R)-2-(tert-butyldimethylsilyloxy)-1-(3-chloro-2-fluorophenyl)ethanamine(369b)

Reaction of (R)-2-amino-2-(3-chloro-2-fluorophenyl)ethanol (369a) (340mg, 1.793 mmol with TBDMS-C₁ (324 mg, 2.152 mmol) according to theprocedure reported in step-1 of Scheme 328 gave after workup(R)-2-(tert-butyldimethylsilyloxy)-1-(3-chloro-2-fluorophenyl)ethanamine(369b) (606 mg) as a white solid which was used as such for next step;MS (ES+): 304.2 & 306.3 (M+1).

Step-2: Preparation of(R)—N-(2-(tert-butyldimethylsilyloxy)-1-(3-chloro-2-fluorophenyl)ethyl)-2-chloroacetamide(369c)

Reaction of(R)-2-(tert-butyldimethylsilyloxy)-1-(3-chloro-2-fluorophenyl)ethanamine(369b) (590 mg, 1.942 mmol) with 2-chloroacetyl chloride (35a) (0.237mL, 2.91 mmol) according to the procedure reported in step-2 of Scheme328 gave after workup(R)—N-(2-(tert-butyldimethylsilyloxy)-1-(3-chloro-2-fluorophenyl)ethyl)-2-chloroacetamide(369c) (495 mg, 74% for two steps) as a colorless gum; ¹H NMR (300 MHz,DMSO-d₆) δ 8.72 (d, J=7.9 Hz, 1H), 7.50 (td, J=7.6, 1.7 Hz, 1H),7.42-7.34 (m, 1H), 7.23 (t, J=7.9 Hz, 1H), 5.18 (q, J=6.9 Hz, 1H), 4.12(s, 2H), 3.85-3.65 (m, 2H), 0.77 (s, 9H), −0.06 (s, 3H), −0.09 (s, 3H);¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.13, −121.14; MS (ES+): 402.2 (M+Na).

Step-3: Preparation ofN—((R)-2-(tert-butyldimethylsilyloxy)-1-(3-chloro-2-fluorophenyl)ethyl)-2-((R)-1-(tert-butyldimethylsilyloxy)propan-2-ylamino)acetamide(369d)

Reaction of(R)—N-(2-(tert-butyldimethylsilyloxy)-1-(3-chloro-2-fluorophenyl)ethyl)-2-chloroacetamide(369c) (480 mg, 1.262 mmol) with(R)-1-(tert-butyldimethylsilyloxy)propan-2-amine (314f) (311 mg, 1.641mmol) according to the procedure reported in step-3 of Scheme 328 gaveafter workup and purification by flash column chromatography [silicagel, eluting with hexanes/ethyl acetate (1:0 to 2:1)]N—((R)-2-(tert-butyldimethylsilyloxy)-1-(3-chloro-2-fluorophenyl)ethyl)-2-((R)-1-(tert-butyldimethylsilyloxy)propan-2-ylamino)acetamide(369d) (376 mg, 56%) as a yellow oil; ¹H NMR (300 MHz, DMSO-d₆) δ 8.36(d, J=8.4 Hz, 1H), 7.56-7.42 (m, 1H), 7.33 (t, J=6.8 Hz, 1H), 7.19 (t,J=7.8 Hz, 1H), 5.27-5.13 (m, 1H), 3.77 (d, J=5.5 Hz, 2H), 3.52-3.34 (m,2H), 3.18 (s, 2H), 2.69-2.55 (m, 1H), 0.94 (d, J=6.3 Hz, 3H), 0.86 (s,9H), 0.78 (s, 9H), 0.03 (s, 3H), 0.02 (s, 3H), −0.08 (s, 3H), −0.11 (s,3H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.43; MS (ES+): 533.4 & 535.4(M+Na).

Step-4: Preparation of tert-butyl1-((R)-10-((R)-1-(tert-butyldimethylsilyloxy)propan-2-yl)-6-(3-chloro-2-fluorophenyl)-2,2,3,3-tetramethyl-8,11-dioxo-4-oxa-7,10-diaza-3-siladodecan-12-yl)-3-carbamoyl-1H-indazol-5-ylcarbamate(369e)

Reaction of2-(5-(tert-butoxycarbonylamino)-3-carbamoyl-1H-indazol-1-yl)acetic acid(345c) (150 mg, 0.449 mmol) withN—((R)-2-(tert-butyldimethylsilyloxy)-1-(3-chloro-2-fluorophenyl)ethyl)-2-((R)-1-(tert-butyldimethylsilyloxy)propan-2-ylamino)acetamide(369d) (299 mg, 0.561 mmol) according to the procedure reported instep-3 of Scheme 2 gave after workup and purification by flash columnchromatography [silica gel, eluting with dichloromethane/methanol (1:0to 19:1)] tert-butyl1-((R)-10-((R)-1-(tert-butyldimethylsilyloxy)propan-2-yl)-6-(3-chloro-2-fluorophenyl)-2,2,3,3-tetramethyl-8,11-dioxo-4-oxa-7,10-diaza-3-siladodecan-12-yl)-3-carbamoyl-1H-indazol-5-ylcarbamate(369e) (342 mg, 90% yield) as an off-white solid; MS (ES+): 849.5 (M+1).

Step-5: Preparation of5-amino-1-(2-((2-((R)-1-(3-chloro-2-fluorophenyl)-2-hydroxyethylamino)-2-oxoethyl)((R)-1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(369f)

Reaction of tert-butyl1-((R)-10-((R)-1-(tert-butyldimethylsilyloxy)propan-2-yl)-6-(3-chloro-2-fluorophenyl)-2,2,3,3-tetramethyl-8,11-dioxo-4-oxa-7,10-diaza-3-siladodecan-12-yl)-3-carbamoyl-1H-indazol-5-ylcarbamate(369e) (300 mg, 0.353 mmol) with conc. HCl (1.177 mL, 14.12 mmol)according to the procedure reported in step-4 of Scheme 360 gave afterworkup and purification by reverse-phase column chromatography elutingwith water (0.1% HCl)/acetonitrile (1:0 to 1:1)5-amino-1-(2-((2-((R)-1-(3-chloro-2-fluorophenyl)-2-hydroxyethylamino)-2-oxoethyl)((R)-1-hydroxypropan-2-yl)amino)-2-oxoethyl)-1H-indazole-3-carboxamide(369f) (9 mg, 5% yield) as an off-white solid; ¹H NMR (300 MHz, DMSO-d₆)(a mixture of two rotamers) δ 9.02 (d, J=7.9 Hz) and 8.59 (d, J=7.8 Hz)(2d, 1H), 8.02 (s, 1H), 7.78 (s, 1H), 7.61-6.98 (m, 6H), 5.70-5.33 (m,2H), 5.30-4.97 (m, 1H), 4.50-3.73 (m, 3H), 3.63 (d, J=6.4 Hz) and 3.53(d, J=6.1 Hz) (2d, 2H), 1.14 (d, J=6.4 Hz) and 0.99 (d, J=6.9 Hz) (2d,3H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −121.61, −121.76; MS (ES+): 543.2 &545.3 (M+Na); MS (ES−): 555.3 & 557.1 (M+Cl).

Example 370

The IC₅₀ value of a compound (i.e., the concentration of the compoundthat inhibits 50% of the enzymatic activity) was calculated according tothe procedure reported in U.S. Pat. No. 6,653,340 B1, e.g., column 74(incorporated by reference).

Specifically, the compounds were dissolved in a stock solution of DMSOat 10.0 or 100 mM. A portion of this stock solution was added to assaybuffer in a final volume of 50 μL. Controls included buffer alone andenzyme solutions to which DMSO was added. Substrate was added to thereaction wells immediately or after incubation at room temperature. Thereaction rates were measured spectrophotometrically by the generation ofproduct at 405 nm for 200 sec. Background absorbance at 690 nm wasmeasured and subtracted from the absorbance at 405 nm for each well.

The reaction rate for enzyme alone was compared to the rate of enzyme inthe presence of inhibitor and the percent inhibition was calculated asshown below:

Percent Inhibition=[Rate without inhibitor−Rate with inhibitor)/(Ratewithout inhibitor)]×100

Factor D Esterolytic Assay:

An established esterolytic assay for the measurement of Factor Dactivity and inhibition of Factor D activity was used (Kam, C. M.;McRae, B. J.; Harper, J. W.; Niemann, M. A.; Volanakis, J. E.; Powers,J. C. Human complement proteins D, C2, and B Active site mapping withpeptide thioester substrates. J Biol. Chem. 1987, 262, 3444-3451). Forthis assay Z-Lys-SBzl, 1.29 mM (Kim, S.; Narayana, S. V. L; Volanakis,J. E. Mutational analysis of the substrate binding site of humancomplement Factor D. Biochemistry. 1994, 33, 14393-14399.) was used asthe substrate for Factor D (104 mM). Hydrolysis of this compound byFactor D liberated a free sulfhydryl group which is then reacted with5,5′-dithiobis(2nitrobenzoic acid) producing an intense yellow color(Habeeb, A. F. S. A. Reaction of protein sulfhydryl groups with Ellman'sReagent. Methods in Enzymol. 1976, 25, 457-464.). The assays wereperformed in 96 well microtiter plates and rates of hydrolysis weremonitored at 405 nm on a Biotek Synergy H1 plate reader. Hydrolysisrates were reported as change in mOD/min. The assay was conducted in 100mM HEPES, 500 mM NaCl, pH 7.5 containing 10% DMSO in a final volume of50 μL per well.

An IC₅₀, a compound concentration which inhibits 50% of the enzymaticactivity, was calculated. Compounds in the examples were tested aminimum of three times. In the table below, three plus symbols (+++) areused to indicate compounds with an IC₅₀ value of less than 1 micromolar;two plus symbols (++) indicate compounds with an IC₅₀ value between 1and 10 micromolar; and one plus symbol (+) indicates compounds with anIC₅₀ value greater than 10 micromolar.

TABLE 1 Measured Ki (IC₅₀) values for compounds. Compound IC₅₀  2f ++ 3d +  4d +  5d ++  6d +  7d +++  8d ++  9e ++  10c +++  11b +++  12d + 13d +  14d +  15d +  16d ++  17a +++  18d +  19d +++  20d +  21d + 22d +  23b +  24b ++  25a +++  26d ++  27d ++  28c +++  29b ++  30b ++ 31d ++  32b +  33b +++  34d +  35d +++  36b +++  37b +++  38b +++ 39f +  40b ++  41b +++  42b +++  43g +  44f ++  45f ++  46b +  47d + 48b +++  49b +++ 142f +  50d +  51b ++  52b +  53b +++  54b ++  55a ++ 56d ++  57d +  58b +++  59d +++  60a ++  61b +++  62b +++  63a ++ 43f +  64b +++  65a ++  66d +  67a +  68a ++  69d +++  70b +++  81b +++ 72b +++  73b +++  74b ++  75b +  76b ++  77b ++  78a +  79a +++  80b+++ 143e + 149f +  81b +++  82e +  83d +  84e +  85b ++  86d +  87a + 88b +  89c ++  90d +++  91a ++  92a ++  93b +  94b +  95b +++  96a ++ 97c +++  98b +++  99e +++ 100a +++ 101a +++ 102b ++ 103a +++ 104b +++105a +++ 106a +++ 107c +++ 108a +++ 109a +++ 110b +++ 111a +++ 112a +++113b +++ 114a +++ 115d +++ 116a +++ 117e +++ 118b +++ 119b ++ 120b +++121b +++ 122b +++ 123b ++ 189a +++ 190a +++ 124e ++ 125a ++ 126a ++ 127a++ 128c +++ 129e +++ 130a +++ 131a +++ 132g +++ 133c +++ 134a +++ 135a+++ 136a +++ 137e +++ 138a ++ 139d ++ 140a ++ 141c +++ 144a + 145b +++146b + 147b +++ 148a +++ 150a +++ 151a +++ 152b +++ 154d +++ 155d +++156f +++ 157c +++ 153a +++ 151a +++ 160a +++ 161c +++ 129b +++ 129c ++164a +++ 162a +++ 163a +++ 165c +++ 166a +++ 167b + 214e +++ 168b ++169c +++ 170b +++ 171b +++ 172b +++ 158a +++ 173b +++ 174a +++ 175a +++176a ++ 177a +++ 178a +++ 179c +++ 180a +++ 181b + 182a +++ 183a +++184b +++ 185b +++ 186b +++ 187c +++ 200i ++ 191a +++ 192a +++ 193a +++194a +++ 195b +++ 196a +++ 197a ++ 201d ++ 202e +++ 203c ++ 204a ++ 205a++ 229c +++ 206d +++ 207g +++ 209b +++ 210b +++ 211a +++ 212a +++ 213a+++ 215a +++ 217b +++ 218a +++ 219b +++ 208a +++ 220a +++ 221a +++ 216a++ 222b +++ 223c +++ 224a +++ 225a +++ 226a +++ 227a +++ 230c +++ 231e+++ 232c +++ 233a +++ 234b +++ 235b +++ 236b +++ 237a +++ 238a +++ 161b++ 198a +++ 228a ++ 231b + 199a + 241a +++ 242a +++ 239b +++ 240f +++243f +++ 244c +++ 245a +++ 246a +++ 247a +++ 248a +++ 249a +++ 250a +++252a + 251a +++ 253a +++ 254d +++ 255b +++ 256a +++ 257a +++ 258a +++259a +++ 264b ++ 260a +++ 261a +++ 262a +++ 263a +++ 188a +++ 265a +++266a +++ 254a +++ 254b + 272a +++ 273a +++ 267c +++ 268c +++ 269a +++270a +++ 271a +++ 274a +++ 275a +++ 276a +++ 282e +++ 283a +++ 286a +++287a +++ 288a +++ 277a +++ 284i +++ 278a +++ 285a ++ 279a +++ 280b +++281c +++ 289a ++ 290a +++ 291h +++ 284g + 292d +++ 294a +++ 293a +++282d +++ 295e +++ 296f +++ 297a + 298b +++ 299a +++ 300a +++ 301h +++302d +++ 303a +++ 304a +++ 305a +++ 306a ++ 307a +++ 308e +++ 309a +++310a +++ 311a +++ 312a +++ 313a +++ 314i +++ 315a +++ 316f +++ 317a +++318b +++ 319a +++ 320a +++ 321a +++ 322b +++ 323a +++ 324b +++ 325b +++267d +++ 326b ++ 327a +++ 328f +++ 328g +++ 329f +++ 330b +++ 331b +++332c ++ 333a +++ 334a +++ 335b +++ 336e +++ 337d +++ 338c +++ 339d ++340c +++ 341a +++ 342d +++ 343b +++ 344e +++ 345e +++ 346d +++ 347b +++348b +++ 349d +++ 350c +++ 351b +++ 352b +++ 353b +++ 354b +++ 355f +++356c +++ 357a +++ 358f ++ 359f + 360d ++ 361h +++ 362a +++ 363d +++ 364b++ 365b +++ 322a +++ 366f +++ 367g ++ 368a +++ 369f ++

INCORPORATION BY REFERENCE

All of the U.S. patents, and U.S. and PCT published patent applicationscited herein are hereby incorporated by reference.

EQUIVALENTS

The foregoing written specification is considered to be sufficient toenable one skilled in the art to practice the invention. The presentinvention is not to be limited in scope by examples provided, since theexamples are intended as a single illustration of one aspect of theinvention and other functionally equivalent embodiments are within thescope of the invention. Various modifications of the invention inaddition to those shown and described herein will become apparent tothose skilled in the art from the foregoing description and fall withinthe scope of the appended claims. The advantages and objects of theinvention are not necessarily encompassed by each embodiment of theinvention.

1. A compound represented by Formula (I), or a pharmaceuticallyacceptable salt thereof:

wherein, independently for each occurrence: R¹ represents substitutedaryl, heteroaryl, cycloalkyl, or heterocycloalkyl; R² and R³ eachindependently represent H; R⁴ represents H or optionally substitutedalkyl, alkenyl, alkynyl, cycloalkyl, (cycloalkyl)alkyl,heterocycloalkyl, (heterocycloalkyl)alkyl, aralkyl, heteroaralkyl,hydroxyalkyl, or haloalkyl; X represents CH₂; Y is absent or representsCH₂, C(O), CR¹⁵R¹⁶, S(O)₂, or optionally substituted(C₃-C₇)cycloalkylene, arylene, or heteroarylene; R^(a) represents H oroptionally substituted (C₁-C₆)alkyl, (heterocycloalkyl)alkyl, or(C₃-C₇)cycloalkyl; m is an integer from 1-6; n is 0 or 1; R¹⁵ and R¹⁶are each independently selected from the group consisting of H, hydroxy,halogen, —C(O)OR¹⁷, —OR¹⁷, —C(O)NR¹⁷R¹⁸, —NR¹⁷R¹⁸, alkyl, hydroxyalkyl,haloalkyl, alkoxyalkyl, aryl, aralkyl, heteroaryl, heteroaralkyl,cycloalkyl, (cycloalkyl)alkyl, heterocycloalkyl, and(heterocycloalkyl)alkyl, wherein alkyl, aryl, aralkyl, heteroaryl,heteroaralkyl, cycloalkyl, (cycloalkyl)alkyl, heterocycloalkyl, and(heterocycloalkyl)alkyl are optionally substituted with one or moresubstituents selected from the group consisting of —CN, —OR¹⁷, —NR¹⁷R¹⁸,halo, and alkyl; or R¹⁵ and R¹⁶ may be taken together with theintervening atom to form an optionally substituted carbocyclic orheterocyclic ring; R¹⁷ and R¹⁸ are each independently selected from thegroup consisting of H, alkyl, haloalkyl, hydroxyalkyl, alkoxyalkyl,aryl, aralkyl, heteroaryl, heteroaralkyl, cycloalkyl, (cycloalkyl)alkyl,heterocycloalkyl, and (heterocycloalkyl)alkyl; or R¹⁷ and R¹⁸, whenattached to the same atom, may be taken together with the interveningatom to form an optionally substituted heterocyclic ring;

represents

Z¹ represents N; Z² represents CH; Z³ represents C; Z⁴ represents CR⁸;Z⁵ represents CR⁵; Z⁶ represents CR⁶; Z⁷ represents CR⁹; R⁵ and R⁶ eachindependently represent H, halogen, —CN, —NO₂, —OR¹³, —NR¹³R¹⁴,—C(O)R¹³, —C(O)OR¹³, —C(O)NR¹³R¹⁴, —OC(O)R¹³, —NR¹³C(O)R¹⁴,—OC(O)NR¹³R¹⁴, —OC(O)OR¹³, —NR¹³C(O)OR¹⁴, —NR¹³C(O)NR¹³R¹⁴,—OS(O)_(p)(R¹³), —NR¹³S(O)_(p)(R¹⁴), or optionally substituted alkyl,alkenyl, alkynyl, haloalkyl, aralkyl, heteroaralkyl, heteroaryl, aryl,cycloalkyl, (cycloalkyl)alkyl, heterocycloalkyl, or(heterocycloalkyl)alkyl; L represents —H, —CN, —C(O)R⁷, —CH(OH)R⁷, or—S(O)_(p)(alkyl); R⁷, independently for each occurrence, represents H,NH₂, CH₃, OH, CF₃, CH₂OH, (C₁-C₆)alkyl, hydroxy(C₁-C₆)alkyl,(C₁-C₆)alkoxy(C₁-C₆)alkyl, halo(C₁-C₆)alkyl, NH(C₁-C₆)alkyl,N((C₁-C₆)alkyl)₂; R⁸ and R⁹ each independently represent H, halogen,—OR¹³, —NR¹³R¹⁴, —C(O)R¹³, —C(O)OR¹³, —C(O)NR¹³R¹⁴, —OC(O)R¹³,—NR¹³C(O)R¹⁴, —OC(O)NR¹³R¹⁴, —OC(O)OR¹³, —NR¹³C(O)OR¹⁴,—NR¹³C(O)NR¹³R¹⁴, —OS(O)_(p)(R¹³), —NR¹³S(O)_(p)(R¹⁴), or optionallysubstituted alkyl, alkenyl, alkynyl, haloalkyl, aralkyl, heteroaralkyl,heteroaryl, or aryl; or R⁵ and R⁸, or R⁵ and R⁶, or R⁶ and R⁹ may betaken together with the intervening atoms to form an optionallysubstituted heterocyclic or carbocyclic ring; R¹³ and R¹⁴, independentlyfor each occurrence, represent H or optionally substituted alkyl,alkenyl, alkynyl, aryl, aralkyl, heteroaryl, heteroaralkyl, cycloalkyl,(cycloalkyl)alkyl, heterocycloalkyl, or (heterocycloalkyl)alkyl; or,when R¹³ and R¹⁴ are attached to the same atom, R¹³ and R¹⁴ takentogether with the atom may form an optionally substituted heterocyclicring; and p is 0, 1, or
 2. 2. The compound of claim 1, wherein n is 1.3. The compound of claim 1, wherein R¹ represents aryl or heteroaryl,substituted by one or more substituents independently selected from thegroup consisting of halogen, —CN, alkoxy, haloalkoxy, haloalkyl,dialkylamino, heterocycloalkyl, aryl, and heteroaryl; or R¹ representsaryl or heteroaryl, substituted by one or more substituents, at leastone of which is halogen.
 4. (canceled)
 5. The compound of claim 1,wherein Y is absent, Y is CH₂, or Y is CR¹⁵R¹⁶.
 6. (canceled) 7.(canceled)
 8. The compound of claim 5, wherein Y is CR¹⁵R¹⁶, and R¹⁵ andR¹⁶ are selected from the group consisting of H, alkyl, hydroxyalkyl,haloalkyl, alkoxyalkyl, aralkyl, heteroaralkyl, (cycloalkyl)alkyl, and(heterocycloalkyl)alkyl; wherein alkyl, aryl, aralkyl, heteroaryl,heteroaralkyl, cycloalkyl, (cycloalkyl)alkyl, heterocycloalkyl, and(heterocycloalkyl)alkyl are optionally substituted with one or moresubstituents selected from the group consisting of —CN, —OR¹⁷, —NR¹⁷R¹⁸,halo, and alkyl; and further wherein R¹⁷ and R¹⁸ are each independentlyselected from the group consisting of H and alkyl.
 9. (canceled)
 10. Thecompound of claim 1, wherein R⁴ represents H or optionally substitutedalkyl, cycloalkyl, (cycloalkyl)alkyl, heterocycloalkyl, aralkyl,hydroxyalkyl, or haloalkyl.
 11. The compound of claim 1, wherein R⁴represents H or optionally substituted alkyl or cycloalkyl.
 12. Thecompound of claim 1, wherein R^(a) is H.
 13. The compound of claim 1,wherein in is
 1. 14. (canceled)
 15. (canceled)
 16. The compound of claim1, wherein L represents C(O)R⁷.
 17. (canceled)
 18. (canceled)
 19. Thecompound of claim 1, having the structure of Formula (Ib):

20-23. (canceled)
 24. The compound of claim 19, wherein Z⁴ and Z⁷ eachrepresent CH.
 25. The compound of claim 19, wherein Z⁵ represents CR⁵;and Z⁶ represents CR⁶; and R⁵ and R⁶ each independently represent H,halogen, —NR¹³R¹⁴, —C(O)R¹³, —C(O)OR¹³, —C(O)NHR¹⁴, —NHC(O)NR¹³R¹⁴,—NHS(O)₂(R¹⁴), or optionally substituted alkyl, alkenyl, alkynyl,heteroaryl, or aryl.
 26. The compound of claim 25, wherein R⁵ and R⁶each independently represent H or alkyl, alkenyl, alkynyl, heteroaryl,or aryl, optionally substituted with one or more substituents selectedfrom the group consisting of aryl, heteroaryl, silyl, alkyl, amino,alkylamino, dialkylamino, —C(O)(alkyl), and halogen.
 27. The compound ofclaim 25, wherein R¹³ and R¹⁴, independently for each occurrence,represent H or optionally substituted aryl, aralkyl, heteroaryl,heteroaralkyl, cycloalkyl, or (cycloalkyl)alkyl.
 28. The compound ofclaim 16, wherein R⁷ represents NH₂, CH₃, or CF₃.
 29. The compound ofclaim 16, wherein R⁷ represents CH₃.
 30. A pharmaceutical composition,comprising a compound of claim 1; and a pharmaceutically acceptablecarrier.
 31. A method of treating or preventing a disease or conditioncharacterized by aberrant complement system activity, comprisingadministering to a subject in need thereof a therapeutically effectiveamount of a compound of claim
 1. 32. The method of claim 31, wherein thedisease or condition characterized by aberrant complement systemactivity is an immunological disorders, a disease of the central nervoussystem, a neurodegenerative disease or neurological disease, a renaldisease, or a cardiovascular disease. 33-36. (canceled)
 37. The methodof claim 31, wherein the disease or condition characterized by aberrantcomplement system activity is selected from the group consisting ofparoxysmal nocturnal hemoglobinuria, atypical hemolytic uremic syndrome,organ transplant rejection, myasthenia gravis, neuromyelitis optica,membranoproliferative glomerulonephritis, dense-deposit disease, coldagglutinin disease, and catastrophic antiphospholipid syndrome.
 38. Thecompound of claim 1, or a pharmaceutically acceptable salt thereof,selected from the following table: